WO2013144737A2 - Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of c-met protein kinases - Google Patents

Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of c-met protein kinases Download PDF

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WO2013144737A2
WO2013144737A2 PCT/IB2013/051577 IB2013051577W WO2013144737A2 WO 2013144737 A2 WO2013144737 A2 WO 2013144737A2 IB 2013051577 W IB2013051577 W IB 2013051577W WO 2013144737 A2 WO2013144737 A2 WO 2013144737A2
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Prior art keywords
substituted
pyridin
unsubstituted
ylmethyl
triazolo
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PCT/IB2013/051577
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English (en)
French (fr)
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WO2013144737A3 (en
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Swaroop Kumar Venkata Satya VAKKALANKA
Dhanapalan Nagarathnam
Srikant Viswanadha
Meyyappan Muthuppalaniappan
Govindarajulu Babu
Prashant K Bhavar
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Rhizen Pharmaceuticals Sa
Incozen Therapeutics Pvt. Ltd.
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Priority to ES13716061T priority Critical patent/ES2856848T3/es
Priority to CN201380022471.6A priority patent/CN104321322A/zh
Priority to SG11201406185WA priority patent/SG11201406185WA/en
Priority to EA201491520A priority patent/EA026412B1/ru
Priority to AU2013239398A priority patent/AU2013239398B2/en
Priority to US14/389,336 priority patent/US9815831B2/en
Priority to CA2865719A priority patent/CA2865719C/en
Priority to MX2014011750A priority patent/MX359888B/es
Priority to AP2014007966A priority patent/AP3908A/en
Priority to JP2015502481A priority patent/JP6192708B2/ja
Priority to NZ629499A priority patent/NZ629499A/en
Priority to KR1020147030532A priority patent/KR20140144726A/ko
Priority to BR112014024251A priority patent/BR112014024251A8/pt
Priority to KR1020207002779A priority patent/KR102164317B1/ko
Priority to EP13716061.0A priority patent/EP2831073B1/en
Application filed by Rhizen Pharmaceuticals Sa, Incozen Therapeutics Pvt. Ltd. filed Critical Rhizen Pharmaceuticals Sa
Publication of WO2013144737A2 publication Critical patent/WO2013144737A2/en
Publication of WO2013144737A3 publication Critical patent/WO2013144737A3/en
Priority to IL234513A priority patent/IL234513B/en
Priority to PH12014502166A priority patent/PH12014502166B1/en
Priority to HK15105126.9A priority patent/HK1204612A1/xx
Priority to US15/705,005 priority patent/US11066402B2/en
Priority to US17/303,494 priority patent/US20210371416A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • the present invention provides compounds useful as protein kinase modulators, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of kinase mediated diseases or disorders with them.
  • protein kinases represent a set of structurally related phosphoryl transferases having conserved structures and catalytic functions. These enzymes modify proteins by chemically adding phosphate groups (phosphorylation). Phosphorylation involves the removal of a phosphate group from ATP and covalently attaching it to amino acids that have a free hydroxyl group such as serine, threonine or tyrosine. Phosphorylation usually results in a functional change of the target protein (substrate) by altering enzyme activity, cellular localization or association with other proteins. Up to 30% of all proteins may be modified by kinase activity.
  • This class of proteins are classified into subsets depending upon the substrate they act upon, such as tyrosine kinase, serine/theronine kinase, histidine kinase and the like. These proteins can also be classified based on their localization into receptor tyrosine kinases (RTKs) or non-receptor tyrosine kinases.
  • RTKs receptor tyrosine kinases
  • Receptor tyrosine kinases have an extracellular portion, a transmembrane domain, and an intracellular portion, while non-receptor tyrosine kinases are entirely intracellular.
  • Receptor tyrosine kinase mediated signal transduction is typically initiated by an extracellular interaction with a specific growth factor (ligand), followed by receptor dimerization, stimulation of the intrinsic protein tyrosine kinase activity, and phosphorylation of amino acid residues.
  • ligand growth factor
  • receptor dimerization stimulation of the intrinsic protein tyrosine kinase activity
  • phosphorylation of amino acid residues phosphorylation of amino acid residues.
  • the ensuing conformational change leads to the formation of complexes with a spectrum of cytoplasmic signalling molecules and facilitates a myriad of responses such as cell division, differentiation, metabolic effects, and changes in the extracellular microenvironment.
  • Met subfamily c-Met, Ron and Sea.
  • Met subfamily c-Met, Ron and Sea.
  • protein kinases see, Plowman et al., DN&P 7(6): 334-339, 1994, Blume- Jensen, P. et al, Nature, 2001, 411(6835):355-365 and Manning, G. et al., Science, 2002, 298(5600): 1912- 1934.
  • Protein kinases exert their physiological functions through phosphorylation of proteins (or substrates) thereby modulating the cellular activities of the substrate in various biological contexts.
  • Protein kinases are known to control a wide variety of biological processes such as cell growth, survival and differentiation, organ formation and morphogenesis, neovascularisation, tissue repair and regeneration. In addition to their functions in normal tissues/organs, many protein kinases also play specialized roles in a host of human diseases including cancer.
  • a subset of protein kinases (also referred to as oncogenic protein kinases), when dysregulated, can cause tumor formation and growth and contribute to tumor maintenance and progression (Blume- Jensen P et al, Nature, 2001, 411(6835):355-365).
  • oncogenic protein kinases represent one of the largest and most attractive groups of protein targets for therapeutic intervention and drug development.
  • Both receptor and non-receptor protein kinases have been found to be attractive targets for small molecule drug discovery due to their impact on cell physiology and signalling. Dysregulation of protein kinase activity thus leads to altered cellular responses including uncontrolled cell growth associated with cancer.
  • altered kinase signalling is implicated in numerous other pathological diseases. These include, but are not limited to immunological disorders, cardiovascular diseases, inflammatory diseases, and degenerative diseases.
  • VEGFR expression which is important for tumor angiogenesis, is associated with a lower survival rate in lung cancer.
  • Tie-1 kinase expression is inversely correlated to survival in gastric cancer.
  • BCR-AbI expression is an important predictor of response in chronic myelogenous leukemia while Src tyrosine kinase expression is co-related to the stage of colorectal cancer.
  • kinases implicated in cancer are c-Met, RON (recepteur d'rare nantais) receptor, Vascular Endothelial Growth Factor (VEGF) receptor, Epidermal growth factor receptor kinase (EGF-R kinase), Eph receptors, c-Kit, and Flt-3.
  • VEGF Vascular Endothelial Growth Factor
  • EGF Vascular Endothelial Growth Factor
  • EGF-R kinase Epidermal growth factor receptor kinase
  • Eph receptors Eph receptors
  • c-Kit Flt-3.
  • a number of small molecule kinase modulators have found their way into the clinic which either act selectively on either one or multiple kinases. These include Gefitinib (AstraZeneca), a EGFR kinase inhibitor; Gleevec (Novartis), a dual c-Kit and Abl kinase inhibitor approved for the treatment of Chronic Myeloid Leukemia (CML) and gastrointestinal stroma cancers; Dasatinib (BMS), a dual BCR/ABL and Src family tyrosine kinases inhibitor, and Sunitinib (Pfizer) a multi kinase inhibitor targeting PDGF-R,VEGF-R, RET, KIT(CD117), CSF-1R and flt-3.
  • Gefitinib AstraZeneca
  • Gleevec Novartis
  • BMS Dasatinib
  • BMS BCR/ABL and Src family tyrosine kin
  • kinase c-Met
  • RTKs heterodimeric receptor tyrosine kinases
  • c-Met occurs in a wide variety of cell types including epithelial, endothelial and mesenchymal cells where activation of the receptor induces cell migration, invasion, proliferation and other biological activities associated with "invasive cell growth.” As such, signal transduction through c-Met receptor activation is responsible for many of the characteristics of tumor cells.
  • HGF hepatocyte growth factor
  • SF scatter factor
  • Binding of HGF to c-Met induces activation of the receptor via autophosphorylation resulting in an increase of receptor dependent signalling, which promotes cell growth and invasion.
  • Both c-Met and HGF are widely expressed in a variety of organs, but their expression is normally confined to cells of epithelial and mesenchymal origin.
  • Anti-HGF antibodies or HGF antagonists have been shown to inhibit tumor metastasis in vivo (see, Maulik et al., Cytokine & Growth Factor Reviews, 2002, 13, 41-59).
  • Tumor growth progression involves the recruitment of new blood vessels into the tumor as well as invasion, adhesion and proliferation of malignant cells.
  • c-Met over expression has been demonstrated on a wide variety of tumor types including breast, colon, renal, lung, squamous cell myeloid leukemia, hemangiomas, melanomas, astrocytomas, and glioblastomas. Additionally activating mutations in the kinase domain of c-Met have been identified in hereditary and sporadic renal papilloma and squamous cell carcinoma.
  • HGF and/or c-Met are over expressed in significant portions of most human cancers, and are often associated with poor clinical outcomes such as more aggressive disease, disease progression, tumor metastasis and shortened patient survival. Further, patients with high levels of HGF/c-Met proteins are more resistant to chemotherapy and radiotherapy.
  • the c-Met receptor can also be activated in cancer patients through genetic mutations (both germline and somatic) and gene amplification. Although gene amplification and mutations are the most common genetic alterations that have been reported in patients, the receptor can also be activated by deletions, truncations, and gene rearrangement, as well as abnormal receptor processing and defective negative regulatory mechanisms.
  • carcinomas e.g., bladder, breast, cervical, cholangiocarcinoma, colorectal, esophageal, gastric, head and neck, kidney, liver, lung, nasopharygeal, ovarian, pancreas, prostate, thyroid
  • musculoskeletal sarcomas e.g., osteosarcaoma, synovial sarcoma, rhabdomyosarcoma
  • soft tissue sarcomas e.g., MFH/fibrosarcoma, leiomyosarcoma, Kaposi's sarcoma
  • hematopoietic malignancies e.g., multiple myeloma, lymphomas, adult T cell leukemia, acute myelogenous leukemia, chronic myeloid leukemia
  • other neoplasms e.g., glioblastomas,
  • c-Met inhibitors may also be useful in preventative and adjuvant therapy settings.
  • certain cancers e.g., papillary renal cell carcinoma, and some gastric and lung cancers
  • c-Met inhibitors may be treated with c-Met inhibitors as they are believed to be driven by c-Met mutation/genetic alteration and dependent on c-Met for growth and survival. These cancers are expected to be sensitive to treatment.
  • Those agents include anti-HGF and anti-c-Met antibodies, HGF peptide antagonists, decoy c-Met receptor, c-Met peptide antagonists, dominant negative c-Met mutations, c-Met specific antisense oligonucleotides and ribozymes, and selective small molecule c-Met kinase inhibitors (Christensen, J.G. et al., Cancer Lett. 2005, 225(1): 1-26).
  • abnormal HGF/c-Met signalling is also implicated in atherosclerosis, lung fibrosis, renal fibrosis and regeneration, liver diseases, allergic disorders, inflammatory and autoimmune disorders, cerebrovascular diseases, cardiovascular diseases, and conditions associated with organ transplantation.
  • c-Met is thus an attractive target from a clinical perspective mainly because of its upstream localisation which aids in early detection and limiting metastasis and implications in the growth and metastases of most types of cancers.
  • Patent literature belonging to some of these applicants include the following patents and/or patent publications: US 7,446,199; US 7,470,693; US 7,459,562; US 7,439,246; US 7,432 ,373; US 7,348,325; US 7,173,031 ; US 7,314,885; US 7,169,800; US 2010/0105656, US 2009/0012076; US 2008/0312232; US 2008/0161305; US 2007/0244116; US 2007/0225307; US 2007/0054928; US 2007/0179130; US 2007/0254868; US 2007/0191369; US 2006/0173055; US 2006/0135537; US 2005/0148574; US 2005/0137201 ; US 2005/0101650; WO 2009/002806; WO 2008/088881; WO 2008/051805; WO 2008/102870; WO 2008/078085; WO 2008/060866; WO 2008/54702;
  • the c-Met pathway plays an important role in the above described human diseases including cancer. There are no c-Met inhibitors or antagonists that are currently available for treating these human disorders that are characterized by abnormal HGF/c-Met signaling. Therefore, there is a clear unmet medical need for compounds which inhibit c-Met and other kinases.
  • the compounds, compositions, and pharmaceutical methods provided herein help meet this need.
  • the present invention is directed to compounds useful as protein kinase modulators and in particular as inhibitors of c-Met.
  • the compound of the present invention has the formula I:
  • X is CR 1 or N
  • D is substituted or unsubstituted monocyclic aryl or substituted or unsubstituted monocyclic heteroaryl; wherein D is substituted with a group E which is selected from -CONH-0-(CR x R y ) p - OR x , -CONH-(CR x R y ) p -OR x" , -CONH-(CR x R y ) p -NR x R y _CONH-(CR x R y ) p -S(0) q R x -CONH- 0-(CR x R y ) p - [cycloalkyl] -(CR x R y ) p -OR x , -CONH-(CR x R y ) p - [cycloalkyl] -(CR x R y ) p -OR x , -CONH-(CR x R y ) p
  • each occurrence of R a and R b is independently selected from hydrogen, halogen, and substituted or unsubstituted (Ci-e) alkyl, or both R a and R b , together with the carbon atom to which they are attached, form a saturated 3 to 6 member cyclic ring which may optionally include one or more heteroatoms which may be same or different and are selected from O, NR e and S (where R e is R z );
  • Zi is selected from N, NR C and CR C ;
  • Z 2 and Z 3 are independently selected from C or N;
  • R c is absent or selected from hydrogen, hydroxy and halogen; and all other variables are the same as defined above.
  • E is selected from -CONR x -0-(CR x R y ) p -OR x , -CONR x -(CR x R y ) p -OR x ⁇ , -CONR x - (CR x R y ) p -NR x R y _CONR x -(CR x R y ) p -S(0) q R x -CONR x -0-(CR x R y ) p - [cycloalkyl] -(CR x R y ) p - OR x , -CONR x -(CR x R y ) p - [cycloalkyl] -(CR x R y ) p -OR x , -CONR x -(CR x R y ) p - [cycloalkyl] -(CR x R y ) p -OR
  • the bicyclic ring containing ring atoms Z, Zi, Z 2 and Z 3 is quinoline, benzo[d]thiazol-6-yl, or an N-oxide thereof, which is optionally substituted with one or two halogen (e.g., F),
  • R a , R b , and each R c are hydrogen,
  • each R 2 is hydrogen, and
  • D is substituted phenyl.
  • D may be N-(2-Hydroxy-ethoxy)-benzamide (i.e.,Ph-CONH-0- CH 2 CH 2 -OH), where the phenyl group may optionally be further substituted by one, two, or three substituents selected from halogens (e.g., F, or CI), alkyl (e.g., methyl or ethyl) and fluorinated methyl (e.g., -CF 3 ).
  • the 2-hydroxy-ethoxy group (- 0-CH 2 -CH 2 -OH) is at the para-position (relative to the phenyl group attachment to the bicyclic core).
  • the 2-hydroxy ethoxy group is at the para- position (relative to the phenyl group attachment to the bicyclic core), and the phenyl group is substituted at one or both the 3- and 5-positions of the phenyl group with the substituents independently selected from halogens (such as F or CI) or alkyl (such as methyl).
  • D can be
  • the bicyclic ring containing ring atoms Z and Zi in the compound of formula (I-IA) is quinoline or an N-oxide thereof, which is optionally substitued with one or two halogen (e.g., F).
  • the bicyclic ring containing ring atoms Z and Zi in the compound of formula (I-IA) is benzo[d]thiazol-6-yl or an N-oxide thereof, which is optionally substitued with one or two halogen (e.g., F).
  • the monocyclic ring D containing ring atoms X, X 1 X 2 and X 3 in the compound of formula (I-IA) is N-(2-Hydroxy-ethoxy)-benzamide (i.e.,Ph-CONH-0- CH 2 CH 2 -OH), where the phenyl group may optionally be further substituted by one or two substituents selected from halogens (e.g., F, or CI), alkanes (e.g., methyl or etthyl) and fluorinated methyl (e.g., -CF 3 ).
  • halogens e.g., F, or CI
  • alkanes e.g., methyl or etthyl
  • fluorinated methyl e.g., -CF 3
  • each R 2 is hydrogen.
  • the representative compounds of the present invention include those specified below and pharmaceutically acceptable salts thereof.
  • the present invention should not be construed to be limited to them.
  • the representative compounds of the present invention include those specified below and pharmaceutically acceptable salts thereof.
  • the present invention should not be construed to be limited to them.
  • the representative compounds of the present invention include those specified below and pharmaceutically acceptable salts thereof.
  • the present invention should not be construed to be limited to them. 1001. 6-((5-(4-carbamoyl-3,5-difluorophenyl)-3H-[l,2,3]triazolo[4,5-b]pyridin-3-yl)methyl) quinoline 1 -oxide
  • Yet another embodiment of the present invention is a method for treating a proliferative disease via modulation of a protein kinase (such as c-Met) by administering to a patient in need of such treatment an effective amount of at least one compound of formula (I), (IA) or (IA-I) as defined above.
  • a protein kinase such as c-Met
  • Yet another embodiment of the present invention is a method for treating a proliferative disease via modulation of a protein kinase (such as c-Met) by administering to a patient in need of such treatment an effective amount of at least one compound of formula (I), (IA) or (IA-I) as defined above, in combination (simultaneously or sequentially) with at least one other anti-cancer agent.
  • a protein kinase such as c-Met
  • the proliferative disease is cancer.
  • the compounds of formula (I), (IA) or (IA-I) and pharmaceutically acceptable esters or salts thereof can be administered for the treatment, prevention and/or amelioration of c-Met, RON, EGFR or KDR kinase associated diseases or disorders, including but not limited to, cancer and other proliferative diseases or disorders.
  • carcinoma including that of the bladder, breast, colon, kidney, liver, lung, including small cell lung cancer, esophagus, gall bladder, ovary, pancreas, stomach, cervix, thyroid, prostate, and skin, including squamous cell carcinoma;
  • lymphoid lineage • hematopoietic tumors of lymphoid lineage, including leukemia, acute lymphocytic leukemia, acute lymphoblastic leukemia, B-cell lymphoma, T-cell lymphoma, Hodgkin's lymphoma, non-Hodgkins lymphoma, hairy cell lymphoma and Burkett's lymphoma;
  • hematopoietic tumors of myeloid lineage including acute and chronic myelogenous leukemias, myelodysplastic syndrome and promyelocytic leukemia;
  • tumors of mesenchymal origin including fibrosarcoma and rhabdomyosarcoma;
  • tumors of the central and peripheral nervous system including astrocytoma, neuroblastoma, glioma and schwannomas;
  • tumors including melanoma, seminoma, teratocarcinoma, osteosarcoma, xenoderoma pigmentosum, keratoctanthoma, thyroid follicular cancer and Kaposi's sarcoma.
  • inhibitors could act as reversible cytostatic agents which may be useful in the treatment of any disease process which features abnormal cellular proliferation, e.g., benign prostatic hyperplasia, familial adenomatosis polyposis, neuro-fibromatosis, atherosclerosis, pulmonary fibrosis, arthritis, psoriasis, glomerulonephritis, restenosis following angioplasty or vascular surgery, hypertrophic scar formation, inflammatory bowel disease, transplantation rejection, endotoxic shock, and fungal infections.
  • benign prostatic hyperplasia familial adenomatosis polyposis
  • neuro-fibromatosis e.g., atherosclerosis, pulmonary fibrosis, arthritis, psoriasis, glomerulonephritis, restenosis following angioplasty or vascular surgery
  • hypertrophic scar formation e.g., benign prostatic hyperplasia, familial adenomatosis polyposis, neuro-fibromatosis,
  • the compounds of the present invention as modulators of apoptosis are useful in the treatment of cancer (including but not limited to those types mentioned herein above), viral infections (including but not limited to herpe virus, poxvirus, Epstein-Barr virus, Sindbis virus and adenovirus), prevention of AIDS development in HIV-infected individuals, autoimmune diseases (including but not limited to systemic lupus, erythematosus, autoimmune mediated glomerulonephritis, rheumatoid arthritis, psoriasis, inflammatory bowel disease, and autoimmune diabetes mellitus), neurodegenerative disorders (including but not limited to Alzheimer's disease, AIDS-related dementia, Parkinson's disease, amyotrophic lateral sclerosis, retinitis pigmentosa, spinal muscular atrophy and cerebellar degeneration), myelodysplastic syndromes, aplastic anemia, ischemic injury associated with myocardial infarctions, stroke and reperfusion injury, arrhythmia
  • cancer
  • the compounds of present invention can modulate the level of cellular RNA and DNA synthesis. These agents are therefore useful in the treatment of viral infections (including but not limited to HIV, human papilloma virus, herpesvirus, poxvirus, Epstein- Barr virus, Sindbis virus and adenovirus).
  • viral infections including but not limited to HIV, human papilloma virus, herpesvirus, poxvirus, Epstein- Barr virus, Sindbis virus and adenovirus.
  • the compounds of the present invention are useful in the chemoprevention of cancer.
  • Chemoprevention is defined as inhibiting the development of invasive cancer by either blocking the initiating mutagenic event or by blocking the progression of pre-malignant cells that have already suffered an insult or inhibiting tumor relapse.
  • the compounds are also useful in inhibiting tumor angiogenesis and metastasis.
  • One embodiment of the invention is a method of inhibiting tumor angiogenesis or metastasis in a patient in need thereof by administering an effective amount of one or more compounds of the present invention.
  • Another embodiment of the present invention is a method of treating an immune system-related disease (e.g., an autoimmune disease), a disease or disorder involving inflammation (e.g., asthma, chronic obstructive pulmonary disease, rheumatoid arthritis, inflammatory bowel disease, glomerulonephritis, neuroinflammatory diseases, multiple sclerosis, uveitis and disorders of the immune system), cancer or other proliferative disease, a hepatic disease or disorder, a renal disease or disorder.
  • the method includes administering an effective amount of one or more compounds of the present invention.
  • immune disorders include psoriasis, rheumatoid arthritis, vasculitis, inflammatory bowel disease, dermatitis, osteoarthritis, asthma, inflammatory muscle disease, allergic rhinitis, vaginitis, interstitial cystitis, scleroderma, osteoporosis, eczema, allogeneic or xenogeneic transplantation (organ, bone marrow, stem cells and other cells and tissues) graft rejection, graft-versus-host disease, lupus erythematosus, inflammatory disease, type I diabetes, pulmonary fibrosis, dermatomyositis, Sjogren's syndrome, thyroiditis (e.g., Hashimoto's and autoimmune thyroiditis), myasthenia gravis, autoimmune hemolytic anemia, multiple sclerosis, cystic fibrosis, chronic relapsing hepatitis, primary biliary cirrhosis, allergic conjunc
  • the compounds described herein are used as immunosuppresants to prevent transplant graft rejections, allogeneic or xenogeneic transplantation rejection (organ, bone marrow, stem cells, other cells and tissues), and graft - versus - host disease.
  • transplant graft rejections result from tissue or organ transplants.
  • graft-versus-host disease results from bone marrow or stem cell transplantation.
  • One embodiment is a method of preventing or decreasing the risk of transplant graft rejection, allogeneic or xenogeneic transplantation rejection (organ, bone marrow, stem cells, other cells and tissues), or graft - versus - host disease by administering an effective amount of one or more compounds of the present invention.
  • the compounds of the present invention are also useful in combination (administered together or sequentially) with known anti-cancer treatments such as radiation therapy or with cytostatic or cytotoxic or anticancer agents, such as for example, but not limited to, DNA interactive agents, such as cisplatin or doxorubicin; topoisomerase II inhibitors, such as etoposide; topoisomerase I inhibitors such as CPT-11 or topotecan; tubulin interacting agents, such as paclitaxel, docetaxel or the epothilones (for example ixabepilone), either naturally occurring or synthetic; hormonal agents, such as tamoxifen; thymidilate synthase inhibitors, such as 5-fluorouracil; and anti-metabolites, such as methotrexate, other tyrosine kinase inhibitors such as Iressa and OSI-774; angiogenesis inhibitors; EGF inhibitors; VEGF inhibitors; CDK inhibitors; S
  • the compounds of the present invention are also useful in combination (administered together or sequentially) with one or more steroidal anti-inflammatory drugs, non-steroidal anti-inflammatory drugs (NSAIDs) or Immune Selective Anti-Inflammatory Derivatives (ImSAIDs).
  • NSAIDs non-steroidal anti-inflammatory drugs
  • ImSAIDs Immune Selective Anti-Inflammatory Derivatives
  • the invention further provides a pharmaceutical composition
  • a pharmaceutical composition comprising one or more compounds of the present invention (such as a compound having formula (I), (IA) or (IA-I) together with a pharmaceutically acceptable carrier.
  • the pharmaceutical composition may further comprise one or more of the active ingredients identified above, such as other anti-cancer agents.
  • the pharmaceutical composition includes a therapeutically effective amount of one or more compounds of formula (I), (IA) or (IA-I).
  • Yet another embodiment is a method of treating leukemia in a patient in need thereof by administering a therapeutically effective amount of a compound of the present invention.
  • the compounds of the present invention are effective for treating carcinoma of the bladder, carcinoma of the breast, carcinoma of the colon, carcinoma of the kidney, carcinoma of the liver, carcinoma of the lung, small cell lung cancer, esophageal cancer, gall bladder cancer, ovarian cancer, pancreatic cancer, stomach cancer, cervical cancer, thyroid cancer, prostate cancer, skin cancer, squamous cell carcinoma; cholangiocarcinoma cancer ,tumors of mesenchymal origin, fibrosarcoma, rhabdomyosarcoma; tumors of the central and peripheral nervous system, astrocytoma, neuroblastoma, glioma, schwannoma; melanoma, seminoma, teratocarcinoma, osteosarcoma, xenoderoma pigmentosum, keratoctanthoma, thyroid
  • alkyl refers to a straight or branched hydrocarbon chain radical consisting solely of carbon and hydrogen atoms, containing no unsaturation, having from one to eight carbon atoms, and which is attached to the rest of the molecule by a single bond, e.g., methyl, ethyl, n-propyl, 1-methylethyl (isopropyl), n-butyl, n-pentyl, and 1,1-dimethylethyl (t-butyl).
  • substituted or unsubstituted (Cy) alkyl refers to an alkyl group as defined above having up to 3 carbon atoms
  • substituted or unsubstituted (Ci_ 4 ) alkyl refers to an alkyl group as defined above having up to 4 carbon atoms
  • substituted or unsubstituted (Ci_e) alkyl refers to an alkyl group as defined above having up to 6 carbon atoms.
  • alkenyl refers to an aliphatic hydrocarbon group containing a carbon-carbon double bond and which may be a straight or branched or branched chain having about 2 to about 10 carbon atoms, e.g., ethenyl, 1-propenyl, 2-propenyl (allyl), iso- propenyl, 2-methyl- 1-propenyl, 1-butenyl, and 2-butenyl.
  • substituted or unsubstituted (Ci_e) alkenyl refers to an alkenyl group as defined above having up to 4 carbon atoms.
  • alkynyl refers to a straight or branched chain hydrocarbyl radicals having at least one carbon-carbon triple bond, and having in the range of about 2 up to 12 carbon atoms (with radicals having in the range of about 2 up to 10 carbon atoms presently being preferred) e.g., ethynyl, propynyl, and butnyl.
  • substituted or unsubstituted (Ci_e) alkynyl refers to an alkynyl group as defined above having up to 4 carbon atoms.
  • alkoxy denotes an alkyl group as defined above attached via an oxygen linkage to the rest of the molecule. Representative examples of these groups are - OCH 3 and -OC 2 H5.
  • substituted alkoxy refers to an alkoxy group where the alkyl constituent is substituted (i.e., -0-(substituted alkyl) wherein the term “substituted alkyl” is the same as defined above for “alkyl”.
  • alkoxy refers to the group -O-alkyl, including from 1 to 8 carbon atoms of a straight, branched, cyclic configuration and combinations thereof attached to the parent structure through oxygen. Examples include methoxy, ethoxy, propoxy, isopropoxy, cyclopropyloxy, and cyclohexyloxy.
  • C 1-3 alkoxy refers to an alkoxy group as defined above having up to 3 atoms.
  • cycloalkyl denotes a non-aromatic mono or multicyclic ring system of about 3 to 12 carbon atoms such as cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.
  • multicyclic cycloalkyl groups include perhydronapththyl, adamantyl and norbornyl groups, bridged cyclic groups, and sprirobicyclic groups, e.g., sprio (4,4) non-2-yl.
  • C3-8 cycloalkyl refers to a cycloalkyl group as defined above having up to 6 atoms.
  • cycloalkylalkyl refers to a cyclic ring-containing radical containing in the range of about 3 up to 8 carbon atoms directly attached to an alkyl group which are then attached to the main structure at any carbon from alkyl group that results in the creation of a stable structure such as cyclopropylmethyl, cyclobuyylethyl, and cyclopentylethyl.
  • C3_6 cycloalkylalkyl refers to a cycloalkylalkyl group as defined above having up to 6 atoms.
  • cycloalkenyl refers to cyclic ring-containing radicals containing in the range of about 3 up to 8 carbon atoms with at least one carbon-carbon double bond, such as cyclopropenyl, cyclobutenyl, and cyclopentenyl.
  • cycloalkenylalkyl refers to a cycloalkenyl group directly attached to an alkyl group which are then attached to the main structure at any carbon from alkyl group that results in the creation of a stable structure
  • C3_6 cycloalkenyl refers to a cycloalkenyl group as defined above having up to 6 atoms.
  • aryl refers to aromatic radicals having in the range of 6 up to 20 carbon atoms such as phenyl, naphthyl, tetrahydronapthyl, indanyl, and biphenyl.
  • arylalkyl refers to an aryl group as defined above directly bonded to an alkyl group as defined above, e.g., -CH 2 C 6 H5 and -C 2 H5C 6 H5.
  • heterocyclic ring refers to a non-aromatic 3 to 15 member ring radical which, consists of carbon atoms and at least one heteroatom selected from the group consisting of nitrogen, phosphorus, oxygen and sulfur.
  • the heterocyclic ring radical may be a mono-, bi-, tri- or tetracyclic ring system, which may include fused, bridged or spiro ring systems, and the nitrogen, phosphorus, carbon, oxygen or sulfur atoms in the heterocyclic ring radical may be optionally oxidized to various oxidation states.
  • the nitrogen atom may be optionally quaternized.
  • the heterocyclic ring radical may be attached to the main structure at any heteroatom or carbon atom that results in the creation of a stable structure.
  • heterocyclyl refers to a heterocylic ring radical as defined above.
  • the heterocylcyl ring radical may be attached to the main structure at any heteroatom or carbon atom that results in the creation of a stable structure.
  • heterocyclylalkyl refers to a heterocylic ring radical as defined above directly bonded to an alkyl group.
  • the heterocyclylalkyl radical may be attached to the main structure at carbon atom in the alkyl group that results in the creation of a stable structure.
  • heterocycloalkyl radicals include, but are not limited to, dioxolanyl, thienyl[l,3]dithianyl, decahydroisoquinolyl, imidazolinyl, imidazolidinyl, isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl, octahydroisoindolyl, 2- oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, oxazolidinyl, piperidinyl, piperazinyl, 4- piperidonyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl, thiazolidinyl, tetrahydrofuryl, trithianyl, tetrahydropyranyl, thiomorpholinyl, thiamorpholinyl, 1-oxox
  • heteroaryl refers to an optionally substituted 5 to 14 member aromatic ring having one or more heteroatoms selected from N, O, and S as ring atoms.
  • the heteroaryl may be a mono-, bi- or tricyclic ring system.
  • heterocyclic ring or “heteroaryl” radicals include, but are not limited to, oxazolyl, thiazolyl, imidazolyl, pyrrolyl, furanyl, pyridinyl, pyrimidinyl, pyrazinyl, benzofuranyl, indolyl, benzothiazolyl, benzoxazolyl, carbazolyl, quinolyl , isoquinolyl, azetidinyl, acridinyl, benzodioxolyl, benzodioxanyl, benzofuranyl, carbazolyl, cinnolinyl, dioxolanyl, indolizinyl, naphthyridinyl, perhydroazepinyl, phenazinyl, phenothiazinyl, phenoxazinyl, phthalazinyl, pteridinyl, purinyl,
  • heteroaryl ring radical may be attached to the main structure at any heteroatom or carbon atom that results in the creation of a stable structure.
  • substituted heteroaryl also includes ring systems substituted with one or more oxide (-0-) substituents, such as pyridinyl N-oxides.
  • heteroarylalkyl refers to heteroaryl ring radical as defined above directly bonded to an alkyl group.
  • the heteroarylalkyl radical may be attached to the main structure at any carbon atom from alkyl group that results in the creation of a stable structure.
  • heterocyclylalkyl refers to a heterocylic ring radical as defined above directly bonded to an alkyl group.
  • the heterocyclylalkyl radical may be attached to the main structure at carbon atom in the alkyl group that results in the creation of a stable structure.
  • cyclic ring refers to a cyclic ring containing 3-10 carbon atoms.
  • Substitution or the combinations of substituents envisioned by this invention are preferably those that result in the formation of a stable or chemically feasible compound.
  • stable refers to the compounds or the structure that are not substantially altered when subjected to conditions to allow for their isolation, production, detection and preferably their recovery, purification and incorporation into a pharmaceutical composition.
  • halo means fluoro, chloro, bromo or iodo.
  • haloalkyl means fluoro, chloro, bromo or iodo.
  • haloalkenyl means fluoro, chloro, bromo or iodo.
  • haloalkynyl means alkyl, alkenyl, alkynyl and alkoxy structures that are substituted with one or more halo groups or with combinations thereof.
  • fluoroalkyl and fluoroalkoxy include haloalkyl and haloalkoxy groups, respectively, in which the halo is fluorine.
  • protecting group refers to a substituent that is employed to block or protect a particular functionality. Other functional groups on the compound may remain reactive.
  • an "amino-protecting group” is a substituent attached to an amino group that blocks or protects the amino functionality in the compound. Suitable amino- protecting groups include, but are not limited to, acetyl, trifluoroacetyl, tert-butoxycarbonyl (BOC), benzyloxycarbonyl (CBz) and 9-fluorenylmethylenoxycarbonyl (Fmoc).
  • a "hydroxy-pro tec ting group” refers to a substituent of a hydroxy group that blocks or protects the hydroxy functionality.
  • Suitable hydroxy-protecting groups include, but are not limited to, acetyl and silyl.
  • a "carboxy-protecting group” refers to a substituent of the carboxy group that blocks or protects the carboxy functionality.
  • Suitable carboxy-protecting groups include, but are not limited to, -CH 2 CH 2 SO 2 PI1, cyanoethyl, 2-(trimethylsilyl)ethyl, 2- (trimethylsilyl)ethoxymethyl, - 2-(p-toluenesulfonyl)ethyl, 2-(p-nitrophenylsulfenyl)ethyl, 2- (diphenylphosphino)-ethyl, and nitroethyl.
  • protecting groups and their use see T. W. Greene, Protective Groups in Organic Synthesis, John Wiley & Sons, New York, 1991.
  • stereoisomer refers to compounds, which have identical chemical composition, but differ with regard to arrangement of the atoms and the groups in space. These include enantiomers, diastereomers, geometrical isomers, atropisomer or conformational isomers.
  • tautomers refers to compounds, which are characterized by relatively easy interconversion of isomeric forms in equilibrium. These isomers are intended to be covered by this invention.
  • “Tautomers” are structurally distinct isomers that interconvert by tautomerization.
  • “Tautomerization” is a form of isomerization and includes prototropic or proton-shift tautomerization, which is considered a subset of acid-base chemistry.
  • Prototropic tautomerization or “proton-shift tautomerization” involves the migration of a proton accompanied by changes in bond order, often the interchange of a single bond with an adjacent double bond. Where tautomerization is possible (e.g.
  • tautomerization is keto-enol tautomerization.
  • keto-enol tautomerization is the interconversion of pentane-2,4-dione and 4-hydroxypent-3-en-2-one tautomers.
  • phenol-keto tautomerization is a specific example of phenol-keto tautomerization.
  • phenol-keto tautomerization is the interconversion of pyridin-4-ol and pyridin-4(lH)-one tautomers.
  • a "leaving group or atom” is any group or atom that will, under the reaction conditions, cleave from the starting material, thus promoting reaction at a specified site. Suitable examples of such groups unless otherwise specified are halogen atoms and mesyloxy, p-nitrobenzensulphonyloxy and tosyloxy groups.
  • prodrug refers to a compound, which is an inactive precursor of a compound, converted into its active form in the body by normal metabolic processes. Prodrug design is discussed generally in Hardma, et al. (Eds.), Goodman and Oilman's The Pharmacological Basis of Therapeutics, 9th ed., pp. 11-16 (1996). A thorough discussion is provided in Higuchi, et al., Prodrugs as Novel Delivery Systems, Vol. 14, ASCD Symposium Series, and in Roche (ed.), Bioreversible Carriers in Drug Design, American Pharmaceutical Association and Pergamon Press (1987).
  • prodrugs can be converted into a pharmacologically active form through hydrolysis of, for example, an ester or amide linkage, thereby introducing or exposing a functional group on the resultant product.
  • the prodrugs can be designed to react with an endogenous compound to form a water-soluble conjugate that further enhances the pharmacological properties of the compound, for example, increased circulatory half-life.
  • prodrugs can be designed to undergo covalent modification on a functional group with, for example, glucuronic acid, sulfate, glutathione, amino acids, or acetate.
  • the resulting conjugate can be inactivated and excreted in the urine, or rendered more potent than the parent compound.
  • High molecular weight conjugates also can be excreted into the bile, subjected to enzymatic cleavage, and released back into the circulation, thereby effectively increasing the biological half-life of the originally administered compound.
  • ester refers to a compound, which is formed by reaction between an acid and an alcohol with elimination of water.
  • An ester can be represented by the general formula RCOOR'.
  • the instant invention also includes the compounds which differ only in the presence of one or more isotopically enriched atoms for example replacement of hydrogen with deuterium or tritium, or the replacement of a carbon by 13C - or 14C -enriched carbon.
  • the compounds of the present invention may also contain unnatural proportions of atomic isotopes at one or more of atoms that constitute such compounds.
  • the compounds may be radiolabeled with radioactive isotopes, such as for example tritium ( 3 H), iodine-125 ( 125 I) or carbon-14 ( 14 C). All isotopic variations of the compounds of the present invention, whether radioactive or not, are encompassed within the scope of the present invention.
  • Pharmaceutically acceptable salts forming part of this invention include salts derived from inorganic bases such as Li, Na, K, Ca, Mg, Fe, Cu, Zn, and Mn; salts of organic bases such as ⁇ , ⁇ '-diacetylethylenediamine, glucamine, triethylamine, choline, hydroxide, dicyclohexylamine, metformin, benzylamine, trialkylamine, and thiamine; chiral bases such as alkylphenylamine, glycinol, and phenyl glycinol; salts of natural amino acids such as glycine, alanine, valine, leucine, isoleucine, norleucine, tyrosine, cystine, cysteine, methionine, proline, hydroxy proline, histidine, ornithine, lysine, arginine, and serine; quaternary ammonium salts of the compounds of invention with alky
  • Salts may include acid addition salts where appropriate which are sulphates, nitrates, phosphates, perchlorates, borates, hydrohalides, acetates, tartrates, maleates, citrates, fumarates, succinates, palmoates, methanesulphonates, benzoates, salicylates, benzenesulfonates, ascorbates, glycerophosphates, and ketoglutarates.
  • acid addition salts where appropriate which are sulphates, nitrates, phosphates, perchlorates, borates, hydrohalides, acetates, tartrates, maleates, citrates, fumarates, succinates, palmoates, methanesulphonates, benzoates, salicylates, benzenesulfonates, ascorbates, glycerophosphates, and ketoglutarates.
  • HGFR is hepatocyte growth factor receptor
  • AIDS Acquired Immuno Deficiency Syndrome
  • HIV Human Immunodeficiency Virus
  • Mel Methyl Iodide
  • POCI 3 Phosphorous Oxychloride
  • KCNS Potassium IsoThiocyanate
  • TLC Thin Layer Chromatography
  • MeOH Methanol
  • CHCI 3 Chloroform.
  • cell proliferation refers to a phenomenon by which the cell number has changed as a result of division. This term also encompasses cell growth by which the cell morphology has changed (e.g., increased in size) consistent with a proliferative signal.
  • co-administration encompasses administration of two or more agents to an animal so that both agents and/or their metabolites are present in the animal at the same time.
  • Co-administration includes simultaneous administration in separate compositions, administration at different times in separate compositions, or administration in a composition in which both agents are present.
  • the term "effective amount” or “therapeutically effective amount” refers to that amount of a compound described herein that is sufficient to effect the intended application including but not limited to disease treatment, as defined below.
  • the therapeutically effective amount may vary depending upon the intended application (in vitro or in vivo), or the subject and disease condition being treated, e.g., the weight and age of the subject, the severity of the disease condition, the manner of administration and the like, which can readily be determined by one of ordinary skill in the art.
  • the term also applies to a dose that will induce a particular response in target cells, e.g. reduction of platelet adhesion and/or cell migration.
  • the specific dose will vary depending on the particular compounds chosen, the dosing regimen to be followed, whether it is administered in combination with other compounds, timing of administration, the tissue to which it is administered, and the physical delivery system in which it is carried.
  • treatment As used herein, “treatment,” “treating,” or “ameliorating” are used interchangeably. These terms refers to an approach for obtaining beneficial or desired results including but not limited to therapeutic benefit and/or a prophylactic benefit.
  • therapeutic benefit is meant eradication or amelioration of the underlying disorder being treated.
  • a therapeutic benefit is achieved with the eradication or amelioration of one or more of the physiological symptoms associated with the underlying disorder such that an improvement is observed in the patient, notwithstanding that the patient may still be afflicted with the underlying disorder.
  • the compositions may be administered to a patient at risk of developing a particular disease, or to a patient reporting one or more of the physiological symptoms of a disease, even though a diagnosis of this disease may not have been made.
  • a prophylactic effect includes delaying or eliminating the appearance of a disease or condition, delaying or eliminating the onset of symptoms of a disease or condition, slowing, halting, or reversing the progression of a disease or condition, or any combination thereof.
  • subject or “patient” refers to an animal, such as a mammal, for example a human. The methods described herein can be useful in both human therapeutics and veterinary applications. In some embodiments, the patient is a mammal, and in some embodiments, the patient is human.
  • Radionuclides e.g., actinium and thorium radionuclides
  • LET low linear energy transfer
  • beta emitters conversion electron emitters
  • high-energy radiation including without limitation x-rays, gamma rays, and neutrons.
  • Signal transduction is a process during which stimulatory or inhibitory signals are transmitted into and within a cell to elicit an intracellular response.
  • a modulator of a signal transduction pathway refers to a compound which modulates the activity of one or more cellular proteins mapped to the same specific signal transduction pathway.
  • a modulator may augment (agonist) or suppress (antagonist) the activity of a signaling molecule.
  • selective inhibition or “selectively inhibit” as applied to a biologically active agent refers to the agent's ability to selectively reduce the target signaling activity as compared to off-target signaling activity, via direct or indirect interaction with the target.
  • compositions include, but is not limited to, any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, one or more suitable diluents, fillers, salts, disintegrants, binders, lubricants, glidants, wetting agents, controlled release matrices, colorants/flavoring, carriers, excipients, buffers, stabilizers, solubilizers, and combinations thereof. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic compositions of the invention is contemplated. Supplementary active ingredients can also be incorporated into the compositions.
  • Inhibition of c-met kinase may be of therapeutic benefit in treatment of various conditions, e.g., conditions characterized by an inflammatory response including but not limited to autoimmune diseases, allergic diseases, and arthritic diseases.
  • "Inflammatory response” as used herein is characterized by redness, heat, swelling and pain (i.e., inflammation) and typically involves tissue injury or destruction.
  • An inflammatory response is usually a localized, protective response elicited by injury or destruction of tissues, which serves to destroy, dilute or wall off (sequester) both the injurious agent and the injured tissue.
  • Inflammatory responses are notably associated with the influx of leukocytes and/or leukocyte (e.g., neutrophil) chemotaxis. Inflammatory responses may result from infection with pathogenic organisms and viruses, noninfectious means such as trauma or reperfusion following myocardial infarction or stroke, immune responses to foreign antigens, and autoimmune diseases. Inflammatory responses amenable to treatment with the methods and compounds according to the invention encompass conditions associated with reactions of the specific defense system as well as conditions associated with reactions of the non-specific defense system.
  • the therapeutic methods of the invention include methods for the amelioration of conditions associated with inflammatory cell activation.
  • “Inflammatory cell activation” refers to the induction by a stimulus (including but not limited to, cytokines, antigens or autoantibodies) of a proliferative cellular response, the production of soluble mediators (including but not limited to cytokines, oxygen radicals, enzymes, prostanoids, or vasoactive amines), or cell surface expression of new or increased numbers of mediators (including but not limited to, major histocompatibility antigens or cell adhesion molecules) in inflammatory cells (including but not limited to monocytes, macrophages, T lymphocytes, B lymphocytes, granulocytes (polymorphonuclear leukocytes including neutrophils, basophils, and eosinophils) mast cells, dendritic cells, Langerhans cells, and endothelial cells).
  • a stimulus including but not limited to, cytokines, antigens or
  • “Autoimmune disease” as used herein refers to any group of disorders in which tissue injury is associated with humoral or cell-mediated responses to the body's own constituents.
  • Transplant rejection refers-to any immune response directed against grafted tissue (including organs or cells (e.g., bone marrow), characterized by a loss of function of the grafted and surrounding tissues, pain, swelling, leukocytosis, and thrombocytopenia).
  • Allergic disease refers to any symptoms, tissue damage, or loss of tissue function resulting from allergy.
  • Articlehritic disease as used herein refers to any disease that is characterized by inflammatory lesions of the joints attributable to a variety of etiologies.
  • Dermatis refers to any of a large family of diseases of the skin that are characterized by inflammation of the skin attributable to a variety of etiologies.
  • the relative efficacies of compounds as inhibitors of an enzyme activity can be established by determining the concentrations at which each compound inhibits the activity to a predefined extent and then comparing the results.
  • the preferred determination is the concentration that inhibits 50% of the activity in a biochemical assay, i.e., the 50% inhibitory concentration or "IC50".
  • IC50 determinations can be accomplished using conventional techniques known in the art. In general, an IC50 can be determined by measuring the activity of a given enzyme in the presence of a range of concentrations of the inhibitor under study. The experimentally obtained values of enzyme activity then are plotted against the inhibitor concentrations used.
  • the concentration of the inhibitor that shows 50% enzyme activity is taken as the IC50 value.
  • other inhibitory concentrations can be defined through appropriate determinations of activity. For example, in some settings it can be desirable to establish a 90% inhibitory concentration, i.e., IC90, etc.
  • a c-met selective inhibitor alternatively can be understood to refer to a compound that exhibits a 50% inhibitory concentration (IC50) with respect to c-met kinase, that is at least 10-fold, in another aspect at least 20-fold, and in another aspect at least 30-fold, lower than the IC50 value with respect to any or all of the other class receptor tyrosine kinase (RTK) family members.
  • IC50 50% inhibitory concentration
  • c-met kinase selective inhibitor can be understood to refer to a compound that exhibits an IC50 with respect to c-met kinase that is at least 50-fold, in another aspect at least 100- fold, in an additional aspect at least 200-fold, and in yet another aspect at least 500-fold, lower than the IC50 with respect to any or all of the other RTK family members.
  • a c-met kinase selective inhibitor is typically administered in an amount such that it selectively inhibits c-met activity, as described above.
  • the methods of the invention may be applied to cell populations in vivo or ex vivo.
  • “In vivo” means within a living individual, as within an animal or human or in a subject's body. In this context, the methods of the invention may be used therapeutically or prophylactically in an individual.
  • "Ex vivo” or “In vitro” means outside of a living individual. Examples of ex vivo cell populations include in vitro cell cultures and biological samples including but not limited to fluid or tissue samples obtained from individuals. Such samples may be obtained by methods known in the art. Exemplary biological fluid samples include blood, cerebrospinal fluid, urine, and saliva. Exemplary tissue samples include tumors and biopsies thereof.
  • the invention may be used for a variety of purposes, including therapeutic and experimental purposes.
  • the invention may be used ex vivo or in vitro to determine the optimal schedule and/or dosing of administration of a c-met kinase selective inhibitor for a given indication, cell type, individual, and other parameters. Information gleaned from such use may be used for experimental or diagnostic purposes or in the clinic to set protocols for in vivo treatment.
  • Other ex vivo uses for which the invention may be suited are described below or will become apparent to those skilled in the art.
  • the invention provides a pharmaceutical composition comprising one or more compounds of the present invention.
  • the pharmaceutical composition may include one or more additional active ingredients as described herein.
  • the pharmaceutical composition may be administered for any of the disorders described herein
  • the invention provides pharmaceutical compositions for treating diseases or conditions related to an undesirable, over-active, harmful or deleterious immune response in a mammal.
  • Such undesirable immune response can be associated with or result in, e.g., asthma, emphysema, bronchitis, psoriasis, allergy, anaphylaxsis, auto-immune diseases, rhuematoid arthritis, graft versus host disease, and lupus erythematosus.
  • the pharmaceutical compositions of the present invention can be used to treat other respiratory diseases including but not limited to diseases affecting the lobes of lung, pleural cavity, bronchial tubes, trachea, upper respiratory tract, or the nerves and muscle for breathing.
  • the invention provides pharmaceutical compositions for the treatment of disorders such as hyperproliferative disorder including but not limited to cancer such as acute myeloid leukemia, thymus, brain, lung, squamous cell, skin, eye, retinoblastoma, intraocular melanoma, oral cavity and oropharyngeal, bladder, gastric, stomach, pancreatic, bladder, breast, cervical, head, neck, renal, kidney, liver, ovarian, prostate, colorectal, esophageal, testicular, gynecological, thyroid, CNS, PNS, AIDS related (e.g. Lymphoma and Kaposi's Sarcoma) or Viral-Induced cancer.
  • cancer such as acute myeloid leukemia, thymus, brain, lung, squamous cell, skin, eye, retinoblastoma, intraocular melanoma, oral cavity and oropharyngeal
  • bladder gastric, stomach, pancreatic, bladder, breast,
  • the pharmaceutical composition is for the treatment of a non-cancerous hyperproliferative disorder such as benign hyperplasia of the skin (e. g., psoriasis), restenosis, or prostate (e. g., benign prostatic hypertrophy (BPH)).
  • a non-cancerous hyperproliferative disorder such as benign hyperplasia of the skin (e. g., psoriasis), restenosis, or prostate (e. g., benign prostatic hypertrophy (BPH)).
  • the invention also relates to a composition for treating a disease related to vasculogenesis or angiogenesis in a mammal which can manifest as tumor angiogenesis, chronic inflammatory disease such as rheumatoid arthritis, inflammatory bowel disease, atherosclerosis, skin diseases such as psoriasis, eczema, and scleroderma, diabetes, diabetic retinopathy, retinopathy of prematurity, age-related macular degeneration, hemangioma, glioma, melanoma, Kaposi's sarcoma and ovarian, breast, lung, pancreatic, prostate, colon and epidermoid cancer.
  • chronic inflammatory disease such as rheumatoid arthritis, inflammatory bowel disease, atherosclerosis, skin diseases such as psoriasis, eczema, and scleroderma
  • diabetes diabetic retinopathy, retinopathy of prematurity
  • the invention also provides compositions for the treatment of liver diseases (including diabetes), pancreatitis or kidney disease (including proliferative glomerulonephritis and diabetes- induced renal disease) or pain in a mammal.
  • liver diseases including diabetes
  • pancreatitis or kidney disease including proliferative glomerulonephritis and diabetes- induced renal disease
  • pain in a mammal.
  • the invention further provides a composition for the prevention of blastocyte implantation in a mammal.
  • the subject pharmaceutical compositions are typically formulated to provide a therapeutically effective amount of a compound of the present invention as the active ingredient, or a pharmaceutically acceptable salt, ester, or prodrug thereof.
  • the pharmaceutical compositions contain a compound of the present invention as the active ingredient or a pharmaceutically acceptable salt and/or coordination complex thereof, and one or more pharmaceutically acceptable excipients, carriers, such as inert solid diluents and fillers, diluents, including sterile aqueous solution and various organic solvents, permeation enhancers, solubilizers and adjuvants.
  • the subject pharmaceutical compositions can be administered alone or in combination with one or more other agents, which are also typically administered in the form of pharmaceutical compositions.
  • the subject compounds and other agent(s) may be mixed into a preparation or both components may be formulated into separate preparations to use them in combination separately or at the same time.
  • Methods include administration of an inhibitor by itself, or in combination as described herein, and in each case optionally including one or more suitable diluents, fillers, salts, disintegrants, binders, lubricants, glidants, wetting agents, controlled release matrices, colorants/flavoring, carriers, excipients, buffers, stabilizers, solubilizers, and combinations thereof.
  • the compounds or pharmaceutical composition of the present invention can be administered by any route that enables delivery of the compounds to the site of action, such asoral routes, intraduodenal routes, parenteral injection (including intravenous, intraarterial, subcutaneous, intramuscular, intravascular, intraperitoneal or infusion), topical administration (e.g. transdermal application), rectal administration, via local delivery by catheter or stent or through inhalation.
  • routes such asoral routes, intraduodenal routes, parenteral injection (including intravenous, intraarterial, subcutaneous, intramuscular, intravascular, intraperitoneal or infusion), topical administration (e.g. transdermal application), rectal administration, via local delivery by catheter or stent or through inhalation.
  • the compounds can also be administered intraadiposally or intrathecally.
  • compositions can be administered in solid, semi-solid, liquid or gaseous form, or may be in dried powder, such as lyophilized form.
  • the pharmaceutical compositions can be packaged in forms convenient for delivery, including, for example, solid dosage forms such as capsules, sachets, cachets, gelatins, papers, tablets, capsules, suppositories, pellets, pills, troches, and lozenges.
  • solid dosage forms such as capsules, sachets, cachets, gelatins, papers, tablets, capsules, suppositories, pellets, pills, troches, and lozenges.
  • the type of packaging will generally depend on the desired route of administration.
  • Implantable sustained release formulations are also contemplated, as are transdermal formulations.
  • the inhibitor compounds may be administered by various routes.
  • pharmaceutical compositions may be for injection, or for oral, nasal, transdermal or other forms of administration, including, e.g., by intravenous, intradermal, intramuscular, intramammary, intraperitoneal, intrathecal, intraocular, retrobulbar, intrapulmonary (e.g., aerosolized drugs) or subcutaneous injection (including depot administration for long term release e.g., embedded-under the-splenic capsule, brain, or in the cornea); by sublingual, anal, or vaginal administration, or by surgical implantation, e.g., embedded under the splenic capsule, brain, or in the cornea.
  • the treatment may consist of a single dose or a plurality of doses over a period of time.
  • the methods of the invention involve administering effective amounts of a modulator of the invention together with one or more pharmaceutically acceptable diluents, preservatives, solubilizers, emulsifiers, adjuvants and/or carriers, as described above.
  • the subject pharmaceutical composition may, for example, be in a form suitable for oral administration as a tablet, capsule, pill, powder, sustained release formulations, solution, suspension, for parenteral injection as a sterile solution, suspension or emulsion, for topical administration as an ointment or cream or for rectal administration as a suppository.
  • the pharmaceutical composition may be in unit dosage forms suitable for single administration of precise dosages.
  • the pharmaceutical composition will include a conventional pharmaceutical carrier or excipient and a compound according to the invention as an active ingredient. In addition, it may include other medicinal or pharmaceutical agents, carriers, and adjuvants.
  • the invention provides methods for oral administration of a pharmaceutical composition of the invention.
  • Oral solid dosage forms are described generally in Remington's Pharmaceutical Sciences, supra at Chapter 89.
  • Solid dosage forms include tablets, capsules, pills, troches or lozenges, and cachets or pellets.
  • liposomal or proteinoid encapsulation may be used to formulate the compositions (as, for example, proteinoid microspheres reported in U.S. Pat. No. 4,925,673).
  • Liposomal encapsulation may include liposomes that are derivatized with various polymers (e.g., U.S. Pat. No. 5,013,556).
  • the formulation may include a compound of the invention and inert ingredients which protect against degradation in the stomach and which permit release of the biologically active material in the intestine.
  • Toxicity and therapeutic efficacy of the met kinase compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., for determining the LD50 (the dose lethal to 50% of the population) and the ED50 (the dose therapeutically effective in 50% of the population). Additionally, this information can be determined in cell cultures or experimental animals additionally treated with other therapies including but not limited to radiation, chemotherapeutic agents, photodynamic therapies, radiofrequency ablation, anti-angiogenic agents, and combinations thereof.
  • an effective dosage is in the range of about 0.001 to about 100 mg per kg body weight per day, preferably about 1 to about 35 mg/kg/day, in single or divided doses. For a 70 kg human, this would amount to about 0.05 to 7 g/day, preferably about 0.05 to about 2.5 g/day. In some instances, dosage levels below the lower limit of the aforesaid range may be more than adequate, while in other cases still larger doses may be employed without causing any harmful side effect, e.g. bydividing such larger doses into several small doses for administration throughout the day.
  • a compound of the invention is administered in a single dose.
  • administration will be by injection, e.g., intravenous injection, in order to introduce the agent quickly.
  • other routes may be used as appropriate.
  • a single dose of a compound of the invention may also be used for treatment of an acute condition.
  • the pharmaceutical compositions are generally provided in doses ranging from 1 pg compound/kg body weight to 1000 mg/kg, 0.1 mg/kg to 100 mg/kg, 0.1 mg/kg to 50 mg/kg, and 1 to 20 mg/kg, given in daily doses or in equivalent doses at longer or shorter intervals, e.g., every other day, twice weekly, weekly, or twice or three times daily.
  • the inhibitor compositions may be administered by an initial bolus followed by a continuous infusion to maintain therapeutic circulating levels of drug product.
  • Those of ordinary skill in the art will readily optimize effective dosages and administration regimens as determined by good medical practice and the clinical condition of the individual to be treated.
  • the frequency of dosing will depend on the pharmacokinetic parameters of the agents and the route of administration.
  • the optimal pharmaceutical formulation will be determined by one skilled in the art depending upon the route of administration and desired dosage [see, for example, Remington's Pharmaceutical Sciences, pp. 1435-1712, the disclosure of which is hereby incorporated by reference]. Such formulations may influence the physical state, stability, rate of in vivo release, and rate of in vivo clearance of the administered agents.
  • a suitable dose may be calculated according to body weight, body surface area or organ size.
  • a compound of the invention is administered in multiple doses. Dosing may be about once, twice, three times, four times, five times, six times, or more than six times per day. Dosing may be about once a month, once every two weeks, once a week, or once every other day. In another embodiment a compound of the invention and another agent are administered together about once per day to about 6 times per day. In another embodiment the administration of a compound of the invention and an agent continues for less than about 7 days. In yet another embodiment the administration continues for more than about 6, 10, 14, 28 days, two months, six months, or one year. In some cases, continuous dosing is achieved and maintained as long as necessary.
  • an agent of the invention is administered for more than 1, 2, 3, 4, 5, 6, 7, 14, or 28 days. In some embodiments, an agent of the invention is administered for less than 28, 14, 7, 6, 5, 4, 3, 2, or 1 day. In some embodiments, an agent of the invention is administered chronically on an ongoing basis, e.g., for the treatment of chronic effects.
  • An effective amount of a compound of the invention may be administered in either single or multiple doses by any of the accepted modes of administration of agents having similar utilities, including rectal, buccal, intranasal and transdermal routes, by intra- arterial injection, intravenously, intraperitoneally, parenterally, intramuscularly, subcutaneously, orally, topically, or as an inhalant.
  • the compounds of the invention may be administered in dosages. It is known in the art that due to intersubject variability in compound pharmacokinetics, individualization of dosing regimen is necessary for optimal therapy. Dosing for a compound of the invention may be found by routine experimentation in light of the instant disclosure.
  • the inhibitors of the invention may be covalently or noncovalently associated with a carrier molecule including but not limited to a linear polymer (e.g., polyethylene glycol, polylysine, dextran, etc.), a branched-chain polymer (see U.S. Pat. Nos. 4,289,872 and 5,229,490; PCT Publication No. WO 93/21259), a lipid, a cholesterol group (such as a steroid), or a carbohydrate or oligosaccharide.
  • a carrier molecule including but not limited to a linear polymer (e.g., polyethylene glycol, polylysine, dextran, etc.), a branched-chain polymer (see U.S. Pat. Nos. 4,289,872 and 5,229,490; PCT Publication No. WO 93/21259), a lipid, a cholesterol group (such as a steroid), or a carbohydrate or oligos
  • carriers for use in the pharmaceutical compositions of the invention include carbohydrate-based polymers such as trehalose, mannitol, xylitol, sucrose, lactose, sorbitol, dextrans such as cyclodextran, cellulose, and cellulose derivatives. Also, the use of liposomes, microcapsules or microspheres, inclusion complexes, or other types of carriers is contemplated.
  • Other carriers include one or more water soluble polymer attachments such as polyoxyethylene glycol, or polypropylene glycol as described U.S. Pat. Nos. 4,640,835, 4,496,689, 4,301,144, 4,670,417, 4,791,192 and 4,179,337.
  • Still other useful carrier polymers known in the art include monomethoxy-polyethylene glycol, poly-(N-vinyl pyrrolidone)- polyethylene glycol, propylene glycol homopolymers, a polypropylene oxidelethylene oxide co-polymer, polyoxyethylated polyols (e.g., glycerol) and polyvinyl alcohol, as well as mixtures of these polymers.
  • Derivitization with bifunctional agents is useful for cross-linking a compound of the invention to a support matrix or to a carrier.
  • a carrier is polyethylene glycol (PEG).
  • PEG polyethylene glycol
  • the PEG group may be of any convenient molecular weight and may be straight chain or branched.
  • the average molecular weight of the PEG can range from about 2 kDa to about 100 kDa, in another aspect from about 5 kDa to about 50 kDa, and in a further aspect from about 5 kDa to about 10 kDa.
  • the PEG groups will generally be attached to the compounds of the invention via acylation, reductive alkylation, Michael addition, thiol alkylation or other chemoselective conjugation/ligation methods through a reactive group on the PEG moiety (e.g., an aldehyde, amino, ester, thiol, ci-haloacetyl, maleimido or hydrazino group) to a reactive group on the target inhibitor compound (e.g., an aldehyde, amino, ester, thiol, a-haloacetyl, maleimido or hydrazino group).
  • a reactive group on the PEG moiety e.g., an aldehyde, amino, ester, thiol, ci-haloacetyl, maleimido or hydrazino group
  • a reactive group on the target inhibitor compound e.g., an aldehyde, amino, ester, thiol,
  • Cross-linking agents can include, e.g., esters with 4-azidosalicylic acid, homobifunctional imidoesters, including disuccinimidyl esters such as 3,3'-dithiobis (succinimidylpropionate), and bifunctional maleimides such as bis-N-maleimido-l,8-octane.
  • Derivatizing agents such as methyl-3-[(p- azidophenyl)dithiolpropioimidate yield photoactivatable intermediates that are capable of forming crosslinks in the presence of light.
  • reactive water-insoluble matrices such as cyanogen bromide-activated carbohydrates and the reactive substrates described in U.S. Pat. Nos. 3,969,287; 3,691,016; 4,195,128; 4,247,642; 4,229,537; and 4,330,440 may be employed for inhibitor immobilization.
  • the invention also provides methods of using the compounds or pharmaceutical compositions of the present invention to treat disease conditions, including but not limited to diseases associated with malfunctioning of c-met kinase and family.
  • the treatment methods provided herein comprise administering to the subject a therapeutically effective amount of a compound of the invention.
  • the present invention provides a method of treating an inflammation disorder, including autoimmune diseases in a mammal. The method comprises administering to said mammal a therapeutically effective amount of a compound of the present invention.
  • disorders, diseases, or conditions treatable with a compound provided herein include, but are not limited to,
  • ⁇ inflammatory or allergic diseases including systemic anaphylaxis and hypersensitivity disorders, atopic dermatitis, urticaria, drug allergies, insect sting allergies, food allergies (including celiac disease and the like), anaphylaxis, serum sickness, drug reactions, insect venom allergies, hypersensitivity pneumonitis, angioedema, erythema multiforme, Stevens-Johnson syndrome, atopic keratoconjunctivitis, venereal keratoconjunctivitis, giant papillary conjunctivitis, and mastocytosis;
  • ⁇ inflammatory bowel diseases including Crohn's disease, ulcerative colitis, ileitis,enteritis, and necrotizing enterocolitis
  • ⁇ psoriasis and inflammatory dermatoses including dermatitis, eczema, , allergic contact dermatitis, , viral cutaneous pathologies including those derived from human papillomavirus, HIV or RLV infection, bacterial, flugal, and other parasital cutaneous pathologies, and cutaneous lupus erythematosus;
  • asthma and respiratory allergic diseases including allergic asthma, exercise induced asthma, allergic rhinitis, otitis media, hypersensitivity lung diseases, chronic obstructive pulmonary disease and other respiratory problems;
  • ⁇ autoimmune diseases and inflammatory conditions including but are not limited to acute disseminated encephalomyelitis (ADEM), Addison's disease, antiphospholipid antibody syndrome (APS), aplastic anemia, autoimmune hepatitis, coeliac disease, Crohn's disease, Diabetes mellitus (type 1), Goodpasture's syndrome, Graves' disease, Guillain-Barre syndrome (GBS), Reynaud's syndrome, Hashimoto's disease, lupus erythematosus, systemic lupus erythematosus (SLE), multiple sclerosis, myasthenia gravis, opsoclonus myoclonus syndrome (OMS), optic neuritis, Ord's thyroiditis, oemphigus, polyarthritis, primary biliary cirrhosis, psoriasis, rheumatoid arthritis, psoriatic arthritis, gouty arthritis, spondylitis,
  • disorders include bone- resorption disorders and thromobsis; tissue or organ transplant rejection disorders including but not limited to graft rejection (including allograft rejection and graft-v-host disease (GVHD)), e.g., skin graft rejection, solid organ transplant rejection, bone marrow transplant rejection; fever; cardiovascular disorders, including acute heart failure, hypotension, hypertension, angina pectoris, myocardial infarction, cardiomyopathy, congestive heart failure, atherosclerosis, coronary artery disease, restenosis, and vascular stenosis; cerebrovascular disorders, including traumatic brain injury, stroke, ischemic reperfusion injury and aneurysm; cancers of the breast, skin, prostate, cervix, uterus, ovary, testes, bladder, lung, liver, larynx, oral cavity, colon and gastrointestinal tract (e.g., esophagus, stomach, pancreas), brain, thyroid, blood, and lymphatic system; fibrosis, connective tissue disease
  • ⁇ pulmonary or respiratory conditions including but not limited to asthma, chronic bronchitis, allergic rhinitis, adult respiratory distress syndrome (ARDS), severe acute respiratory syndrome (SARS), chronic pulmonary inflammatory diseases (e.g., chronic obstructive pulmonary disease), silicosis, pulmonary sarcoidosis, pleurisy, alveolitis, vasculitis, pneumonia, bronchiectasis, hereditary emphysema, and pulmonary oxygen toxicity;
  • chronic pulmonary inflammatory diseases e.g., chronic obstructive pulmonary disease
  • silicosis e.g., chronic obstructive pulmonary disease
  • silicosis e.g., chronic obstructive pulmonary disease
  • silicosis e.g., chronic obstructive pulmonary disease
  • silicosis e.g., chronic obstructive pulmonary disease
  • silicosis e.g., chronic o
  • ischemic -reperfusion injury e.g., of the myocardium, brain, or extremities
  • ⁇ fibrosis including but not limited to cystic fibrosis; keloid formation or scar tissue formation;
  • central or peripheral nervous system inflammatory conditions including but not limited to meningitis (e.g., acute purulent meningitis), encephalitis, and brain or spinal cord injury due to minor trauma;
  • Sjorgren's syndrome diseases involving leukocyte diapedesis; alcoholic hepatitis; bacterial pneumonia; community acquired pneumonia (CAP); Pneumocystis carinii pneumonia (PCP); antigen-antibody complex mediated diseases; hypovolemic shock; acute and delayed hypersensitivity; disease states due to leukocyte dyscrasia and metastasis; thermal injury; granulocyte transfusion associated syndromes; cytokine- induced toxicity; stroke; pancreatitis; myocardial infarction, respiratory syncytial virus (RSV) infection; and spinal cord injury.
  • CAP community acquired pneumonia
  • PCP Pneumocystis carinii pneumonia
  • antigen-antibody complex mediated diseases hypovolemic shock
  • acute and delayed hypersensitivity disease states due to leukocyte dyscrasia and metastasis
  • thermal injury granulocyte transfusion associated syndromes
  • cytokine- induced toxicity stroke
  • pancreatitis myocardial infarction, respiratory
  • the cancer or cancers treatable with the methods provided herein includes, but is or are not limited to,
  • leukemias including, but not limited to, acute leukemia, acute lymphocytic leukemia, acute myelocytic leukemias such as myeloblasts, promyelocyte, myelomonocytic, monocytic, erythroleukemia leukemias and myelodysplastic syndrome or a symptom thereof (such as anemia, thrombocytopenia, neutropenia, bicytopenia or pancytopenia), refractory anemia (RA), RA with ringed sideroblasts (RARS), RA with excess blasts (RAEB), RAEB in transformation (RAEB-T), preleukemia, and chronic myelomonocytic leukemia (CMML); chronic leukemias, including, but not limited to, chronic myelocytic (granulocytic) leukemia, chronic lymphocytic leukemia, and hairy cell leukemia; polycythemia vera; lymphomas, including, but not limited to, Ho
  • kidney cancer including, but not limited to, renal cell cancer, adenocarcinoma,
  • bladder cancer including, but not limited to, transitional cell carcinoma, squamous cell cancer, adenocarcinoma, and carcinosarcoma; and other cancer, including, not limited to, myxosarcoma, osteogenic sarcoma, endotheliosarcoma, lymphangio- endotheliosarcoma, mesothelioma, synovioma, hemangioblastoma, epithelial carcinoma, cystadenocarcinoma, bronchogenic carcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, and papillary adenocarcinomas
  • the treatment methods of the invention are useful in the fields of human medicine and veterinary medicine.
  • the individual to be treated may be a mammal, preferably human, or other animals.
  • individuals include but are not limited to farm animals including cows, sheep, pigs, horses, and goats; companion animals such as dogs and cats; exotic and/or zoo animals; laboratory animals including mice, rats, rabbits, guinea pigs, and hamsters; and poultry such as chickens, turkeys, ducks, and geese.
  • the compounds described herein are used for the treatment of cancer such as acute myeloid leukemia, thymus, brain, lung, squamous cell, skin, eye, retinoblastoma, intraocular melanoma, oral cavity and oropharyngeal, bladder, gastric, stomach, pancreatic, bladder, breast, cervical, head, neck, renal, kidney, liver, ovarian, prostate, colorectal, esophageal, testicular, gynecological, thyroid, CNS, PNS, AIDS-related (e.g. Lymphoma and Kaposi's Sarcoma) or viral-induced cancer.
  • cancer such as acute myeloid leukemia, thymus, brain, lung, squamous cell, skin, eye, retinoblastoma, intraocular melanoma, oral cavity and oropharyngeal, bladder, gastric, stomach, pancreatic, bladder, breast, cervical, head, neck, renal, kidney, liver, ovarian
  • said method relates to the treatment of a non-cancerous hyperproliferative disorder such as benign hyperplasia of the skin (e. g., psoriasis), restenosis, or prostate (e.g., benign prostatic hypertrophy (BPH)).
  • a non-cancerous hyperproliferative disorder such as benign hyperplasia of the skin (e. g., psoriasis), restenosis, or prostate (e.g., benign prostatic hypertrophy (BPH)).
  • the invention also relates to a method of treating diseases related to vasculogenesis or angiogenesis in a mammal that comprises administering to said mammal a therapeutically effective amount of a compound of the present invention.
  • said method is for treating a disease selected from the group consisting of tumor angiogenesis, chronic inflammatory disease such as rheumatoid arthritis, atherosclerosis, inflammatory bowel disease, skin diseases such as psoriasis, eczema, and scleroderma, diabetes, diabetic retinopathy, retinopathy of prematurity, age-related macular degeneration, hemangioma, glioma, melanoma, Kaposi's sarcoma and ovarian, breast, lung, pancreatic, prostate, colon and epidermoid cancer.
  • Patients that can be treated with compounds of the present invention, according to the methods of this invention include, for example, patients that have been diagnosed as having psoriasis; restenosis; atherosclerosis; BPH; breast cancer such as a ductal carcinoma in duct tissue in a mammary gland, medullary carcinomas, colloid carcinomas, tubular carcinomas, and inflammatory breast cancer; ovarian cancer, including epithelial ovarian tumors such as adenocarcinoma in the ovary and an adenocarcinoma that has migrated from the ovary into the abdominal cavity; uterine cancer; cervical cancer such as adenocarcinoma in the cervix epithelial including squamous cell carcinoma and adenocarcinomas; prostate cancer, such as a prostate cancer selected from the following: an adenocarcinoma or an adenocarinoma that has migrated to the bone; pancreatic cancer such as epitheliod carcinoma in the pancreatic
  • the invention also relates to a method of treating diabetes in a mammal that comprises administering to said mammal a therapeutically effective amount of a compound of the present invention.
  • the compounds described herein may be used to treat acne.
  • the compounds described herein may be used for the treatment of arteriosclerosis, including atherosclerosis.
  • Arteriosclerosis is a general term describing any hardening of medium or large arteries.
  • Atherosclerosis is a hardening of an artery specifically due to an atheromatous plaque.
  • the compounds described herein may be used for the treatment of glomerulonephritis.
  • Glomerulonephritis is a primary or secondary autoimmune renal disease characterized by inflammation of the glomeruli. It may be asymptomatic, or present with hematuria and/or proteinuria. There are many recognized types, divided in acute, subacute or chronic glomerulonephritis. Causes are infectious (bacterial, viral or parasitic pathogens), autoimmune or paraneoplastic.
  • the compounds described herein may be used for the treatment of bursitis, lupus, acute disseminated encephalomyelitis (ADEM), addison's disease, antiphospholipid antibody syndrome (APS), aplastic anemia, autoimmune hepatitis, coeliac disease, Crohn's disease, diabetes mellitus (type 1), goodpasture's syndrome, graves' disease, guillain-barre syndrome (GBS), hashimoto's disease, inflammatory bowel disease, lupus erythematosus, myasthenia gravis, opsoclonus myoclonus syndrome (OMS), optic neuritis, ord's thyroiditiSj Osteoarthritis, uveoretinitis, pemphigus, polyarthritis, primary biliary cirrhosis, reiter's syndrome, takayasu's arteritis, temporal arteritis, warm autoimmune hemolytic an
  • the invention also relates to a method of treating a cardiovascular disease in a mammal that comprises administering to said mammal a therapeutically effective amount of a compound of the present invention.
  • cardiovascular conditions include, but are not limited to, atherosclerosis, restenosis, vascular occlusion and carotid obstructive disease.
  • the present invention provides methods of disrupting the function of a leukocyte or disrupting a function of an osteoclast.
  • the method includes contacting the leukocyte or the osteoclast with a function disrupting amount of a compound of the invention.
  • methods are provided for treating ophthalmic disease by administering one or more of the subject compounds or pharmaceutical compositions to the eye of a subject.
  • the invention further provides methods of modulating kinase activity by contacting a kinase with an amount of a compound of the invention sufficient to modulate the activity of the kinase. Modulate can be inhibiting or activating kinase activity. In some embodiments, the invention provides methods of inhibiting kinase activity by contacting a kinase with an amount of a compound of the invention sufficient to inhibit the activity of the kinase. In some embodiments, the invention provides methods of inhibiting kinase activity in a solution by contacting said solution with an amount of a compound of the invention sufficient to inhibit the activity of the kinase in said solution.
  • the invention provides methods of inhibiting kinase activity in a cell by contacting said cell with an amount of a compound of the invention sufficient to inhibit the activity of the kinase in said cell. In some embodiments, the invention provides methods of inhibiting kinase activity in a tissue by contacting said tissue with an amount of a compound of the invention sufficient to inhibit the activity of the kinase in said tissue. In some embodiments, the invention provides methods of inhibiting kinase activity in an organism by contacting said organism with an amount of a compound of the invention sufficient to inhibit the activity of the kinase in said organism.
  • the invention provides methods of inhibiting kinase activity in an animal by contacting said animal with an amount of a compound of the invention sufficient to inhibit the activity of the kinase in said animal. In some embodiments, the invention provides methods of inhibiting kinase activity in a mammal by contacting said mammal with an amount of a compound of the invention sufficient to inhibit the activity of the kinase in said mammal. In some embodiments, the invention provides methods of inhibiting kinase activity in a human by contacting said human with an amount of a compound of the invention sufficient to inhibit the activity of the kinase in said human.
  • the % of kinase activity after contacting a kinase with a compound of the invention is less than 1, 5, 10, 20, 30, 40, 50, 60, 70, 80, 90, 95, or 99% of the kinase activity in the absence of said contacting step.
  • the kinase is a pretein kinase , more particularly a nonreceptor or receptor tyrosine protein kinase.
  • the kinase is selected from the group consisting of C-met including mutants if any; Abl, VEGFR, Ephrin receptor B4 (EphB4); TEK receptor tyrosine kinase (HE2); FMS-related tyrosine kinase 3 (FLT-3); Platelet derived growth factor receptor (PDGFR); RET; ATM; ATR; hSmg-1 ; Hck; Src; Epidermal growth factor receptor (EGFR); KIT; Inulsin Receptor (IR) and IGFR.
  • C-met including mutants if any; Abl, VEGFR, Ephrin receptor B4 (EphB4); TEK receptor tyrosine kinase (HE2); FMS-related tyrosine kinase 3 (FLT-3); Platelet derived growth factor receptor (PDGFR); RET; ATM; ATR; hSmg-1 ; Hck; Src; Epiderma
  • the invention further provides methods of modulating c-met kinase activity by contacting a c-met kinase with an amount of a compound of the invention sufficient to modulate the activity of the c-met kinase. Modulate can be inhibiting or activating c-met kinase activity. In some embodiments, the invention provides methods of inhibiting c-met kinase activity by contacting a c-met kinase with an amount of a compound of the invention sufficient to inhibit the activity of the c-met kinase. In some embodiments, the invention provides methods of inhibiting c-met kinase activity.
  • Such inhibition can take place in solution, in a cell expressing one or more c-met kinase, in a tissue comprising a cell expressing one or more c-met kinases, or in an organism expressing one or more c-met kinase.
  • the invention provides methods of inhibiting c-met kinase activity in an animal (including mammal such as humans) by contacting said animal with an amount of a compound of the invention sufficient to inhibit the activity of the c-met kinase in said animal.
  • the present invention also provides methods for combination therapies in which an agent known to modulate other pathways, or other components of the same pathway, or even overlapping sets of target enzymes are used in combination with a compound of the present invention.
  • such therapy includes but is not limited to the combination of the subject compound with chemotherapeutic agents, therapeutic antibodies, and radiation treatment, to provide a synergistic or additive therapeutic effect.
  • the subject compounds or pharmaceutical compositions can be used in combination with commonly prescribed drugs including but not limited to Enbrel ® , Remicade ® , Humira ® , Avonex ® , and Rebif ® .
  • the subject compounds or pharmaceutical compositions can be administered in combination with commonly prescribed drugs including but not limited to Xolair ® , Advair ® , Singulair ® , and Spiriva ® .
  • the compounds of the invention may be formulated or administered in conjunction with other agents that act to relieve the symptoms of inflammatory conditions such as encephalomyelitis, asthma, and the other diseases described herein.
  • agents include non-steroidal anti-inflammatory drugs (NSAIDs), e.g. acetylsalicylic acid; ibuprofen; naproxen; indomethacin; nabumetone; tolmetin; etc.
  • NSAIDs non-steroidal anti-inflammatory drugs
  • Corticosteroids are used to reduce inflammation and suppress activity of the immune system.
  • the most commonly prescribed drug of this type is Prednisone.
  • Chloroquine (Aralen) or hydroxychloroquine (Plaquenil) may also be very useful in some individuals with lupus.
  • Azathioprine Imuran
  • Cytoxan cyclophosphamide
  • Other agents e.g. methotrexate and cyclosporin are used to control the symptoms of lupus.
  • Anticoagulants are employed to prevent blood from clotting rapidly. They range from aspirin at very low dose which prevents platelets from sticking, to heparin/coumadin.
  • this invention also relates to a pharmaceutical composition for inhibiting abnormal cell growth in a mammal which comprises an amount of a compound of the present invention, in combination with an amount of an anti-cancer agent (e.g. a chemotherapeutic agent).
  • an anti-cancer agent e.g. a chemotherapeutic agent
  • Many chemotherapeutics are presently known in the art and can be used in combination with the compounds of the invention.
  • the chemotherapeutic is selected from the group consisting of mitotic inhibitors, alkylating agents, anti-metabolites, intercalating antibiotics, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, anti-hormones, angiogenesis inhibitors, and anti-androgens.
  • chemotherapeutic agents include cytotoxic agents, and non-peptide small molecules such as Gleevec (Imatinib Mesylate), Velcade (bortezomib), Iressa (gefitinib), Sprycel (Dasatinib), and Adriamycin as well as a host of chemotherapeutic agents.
  • Non-limiting examples of chemotherapeutic agents include alkylating agents such as thiotepa and cyclosphosphamide (CYTOXANTM); alkyl sulfonates such as busulfan, improsulfan and piposulfan; aziridines such as benzodopa, carboquone, meturedopa, and uredopa; ethylenimines and methylamelamines including altretamine, triethylenemelamine, trietylenephosphoramide, triethylenethiophosphaoramide and trimethylolomelamine; nitrogen mustards such as chlorambucil, chlornaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, novembichin, phenesterine, prednimustine, trofosfamide, uracil mustard; nitrosureas such as car
  • paclitaxel TAXOLTM, Bristol-Myers Squibb Oncology, Princeton, NJ.
  • docetaxel TAXOTERETM, Rhone- Poulenc Rorer, Antony, France
  • retinoic acid esperamicins
  • capecitabine ecitabine
  • chemotherapeutic cell conditioners are anti- hormonal agents that act to regulate or inhibit hormone action on tumors such as anti-estrogens including for example tamoxifen (NolvadexTM), raloxifene, aromatase inhibiting 4(5)-imidazoles, 4-hydroxytamoxifen, trioxifene, keoxifene, LY 117018, onapristone, and toremifene (Fareston); and anti- androgens such as flutamide, nilutamide, bicalutamide (Casodex), leuprolide, and goserelin (Zoladex); chlorambucil; gemcitabine; 6-thioguanine; mercaptopurine; methotrexate; platinum analogs such as cisplatin and carboplatin; vinblastine; platinum; etoposide (VP-16); ifosfamide; mitomycin C; mitoxantrone; vincristine;
  • Anti-Her2 antibodies may also be utilized.
  • Suitable EGFR inhibitors include gefitinib, erlotinib, and cetuximab.
  • Pan Her inhibitors include canertinib, EKB-569, and GW-572016.
  • Further suitable anticancer agents include, but are not limited to, Src inhibitors, MEK-1 kinase inhibitors, MAPK kinase inhibitors, PI3 kinase inhibitors, and PDGF inhibitors, such as imatinib.
  • anti-angiogenic and antivascular agents which, by interrupting blood flow to solid tumors, render cancer cells quiescent by depriving them of nutrition.
  • Castration which also renders androgen dependent carcinomas nonproliferative, may also be utilized. Also included are IGF1R inhibitors, inhibitors of nonreceptor and receptor tyrosine kinases, and inhibitors of integrin signalling. Additional anticancer agents include microtubule-stabilizing agents 7-O-methylthiomethylpaclitaxel (disclosed in U.S. Pat. No.
  • CDK inhibitors an antiproliferative cell cycle inhibitor, epidophyllotoxin; an antineoplastic enzyme; biological response modifiers; growth inhibitors; antihormonal therapeutic agents; leucovorin; tegafur; and haematopoietic growth factors.
  • Additional cytotoxic agents include, hexamethyl melamine, idatrexate, L- asparaginase, camptothecin, topotecan, pyridobenzoindole derivatives, interferons, and interleukins.
  • the compounds or pharmaceutical composition of the present invention can be used in combination with commonly prescribed anti-cancer drugs such as Herceptin ® , Avastin ® , Erbitux ® , Rituxan ® , Taxol ® , Arimidex ® , Taxotere ® , and Velcade ®
  • This invention further relates to a method for using the compounds or pharmaceutical composition in combination with radiation therapy in inhibiting abnormal cell growth or treating the hyperproliferative disorder in the mammal.
  • Techniques for administering radiation therapy are known in the art, and these techniques can be used in the combination therapy described herein.
  • the administration of the compound of the invention in this combination therapy can be determined as described herein.
  • Radioactive isotopes e.g. At-211, 1-131, 1-125, Y-90, Re-186, Re-188, Sm-153, Bi-212, P-32, and radioactive isotopes of Lu.
  • Suitable radiation sources for use as a cell conditioner of the present invention include both solids and liquids.
  • the radiation source can be a radionuclide, such as 1-125, 1-131, Yb-169, Ir- 192 as a solid source, 1-125 as a solid source, or other radionuclides that emit photons, beta particles, gamma radiation, or other therapeutic rays.
  • the radioactive material can also be a fluid made from any 5 solution of radionuclides), e.g., a solution of 1-125 or 1-131, or a radioactive fluid can be produced using a slurry of a suitable fluid containing small particles of solid radionuclides, such as Au-198, Y-90.
  • the radionuclide(s) can be embodied in a gel or radioactive micro spheres.
  • the compounds of the present invention can render abnormal cells more sensitive to treatment with radiation for purposes of killing and/or inhibiting the growth of such cells. Accordingly, this invention further relates to a method for sensitizing abnormal cells in a mammal to treatment with radiation which comprises administering to the mammal an amount of a compound of the present invention, which amount is effective is sensitizing abnormal cells to treatment with radiation.
  • the compounds or pharmaceutical compositions of the present invention can be used in combination with an amount of one or more substances selected from anti- angiogenesis agents, signal transduction inhibitors, and antiproliferative agents.
  • Anti-angiogenesis agents such as MMP-2 (matrix-metalloprotienase 2) inhibitors, MMP-9 (matrix- metalloprotienase 9) inhibitors, and COX-H (cyclooxygenase 11) inhibitors, can be used in conjunction with a compound of the present invention and pharmaceutical compositions described herein.
  • MMP-2 matrix-metalloprotienase 2
  • MMP-9 matrix- metalloprotienase 9
  • COX-H cyclooxygenase 11
  • useful COX-II inhibitors include CELEBREXTM (alecoxib), valdecoxib, and rofecoxib.
  • Examples of useful matrix metalloproteinase inhibitors are described in WO 96/33172 (published October 24,1996), WO 96/27583 (published March 7,1996), European Patent Application No.
  • MMP-2 and MMP-9 inhibitors are those that have little or no activity inhibiting MMP-I.
  • the invention also relates to a method of and to a pharmaceutical composition of treating a cardiovascular disease in a mammal which comprises an amount of a compound of the present invention, or an isotopically-labeled derivative thereof, and an amount of one or more therapeutic agents use for the treatment of cardiovascular diseases.
  • anti-thrombotic agents e.g., prostacyclin and salicylates
  • thrombolytic agents e.g., streptokinase, urokinase, tissue plasminogen activator (TPA) and anisoylated plasminogen-streptokinase activator complex (APSAC)
  • anti-platelets agents e.g., acetyl-salicylic acid (ASA) and clopidrogel
  • vasodilating agents e.g., nitrates
  • calcium channel blocking drugs antiproliferative agents, e.g., colchicine and alkylating agents, intercalating agents, growth modulating factors such as interleukins, transformation growth factor-beta and congeners of platelet derived growth factor, monoclonal antibodies directed against growth factors, anti-inflammatory agents, both steroidal and non-steroidal, and other agents that can modulate vessel tone, function,
  • Antibiotics can also be included in combinations or coatings comprised by the invention. Moreover, a coating can be used to effect therapeutic delivery focally within the vessel wall. By incorporation of the active agent in a swellable polymer, the active agent will be released upon swelling of the polymer.
  • exemplary therapeutic agents useful for a combination therapy include but are not limited to agents as described above, radiation therapy, hormone antagonists, hormones and their releasing factors, thyroid and antithyroid drugs, estrogens and progestins, androgens, adrenocorticotropic hormone; adrenocortical steroids and their synthetic analogs; inhibitors of the synthesis and actions of adrenocortical hormones, insulin, oral hypoglycemic agents, and the pharmacology of the endocrine pancreas, agents affecting calcification and bone turnover: calcium, phosphate, parathyroid hormone, vitamin D, calcitonin, vitamins such as water-soluble vitamins, vitamin B complex, ascorbic acid, fat-soluble vitamins, vitamins A, K, and E, growth factors, cytokines, chemokines, muscarinic receptor agonists and antagonists; anticholinesterase agents; agents acting at the neuromuscular junction and/or autonomic ganglia; catecholamines, sympathom
  • Therapeutic agents can also include agents for pain and inflammation such as histamine and histamine antagonists, bradykinin and bradykinin antagonists, 5- hydroxytryptamine (serotonin), lipid substances that are generated by biotransformation of the products of the selective hydrolysis of membrane phospholipids, eicosanoids, prostaglandins, thromboxanes, leukotrienes, aspirin, nonsteroidal anti-inflammatory agents, analgesic-antipyretic agents, agents that inhibit the synthesis of prostaglandins and thromboxanes, selective inhibitors of the inducible cyclooxygenase, selective inhibitors of the inducible cyclooxygenase-2, autacoids, paracrine hormones, somatostatin, gastrin, cytokines that mediate interactions involved in humoral and cellular immune responses, lipid-derived autacoids, eicosanoids, ⁇ -adrenergic agonists, i
  • Additional therapeutic agents contemplated herein include diuretics, vasopressin, agents affecting the renal conservation of water, rennin, angiotensin, agents useful in the treatment of myocardial ischemia, anti-hypertensive agents, angiotensin converting enzyme inhibitors, ⁇ -adrenergic receptor antagonists, agents for the treatment of hypercholesterolemia, and agents for the treatment of dyslipidemia.
  • Other therapeutic agents contemplated include drugs used for control of gastric acidity, agents for the treatment of peptic ulcers, agents for the treatment of gastroesophageal reflux disease, prokinetic agents, antiemetics, agents used in irritable bowel syndrome, agents used for diarrhea, agents used for constipation, agents used for inflammatory bowel disease, agents used for biliary disease, agents used for pancreatic disease.
  • Therapeutic agents used to treat protozoan infections drugs used to treat Malaria, Amebiasis, Giardiasis, Trichomoniasis, Trypanosomiasis, and/or Leishmaniasis, and/or drugs used in the chemotherapy of helminthiasis.
  • therapeutic agents include antimicrobial agents, sulfonamides, trimethoprim-sulfamethoxazole quinolones, and agents for urinary tract infections, penicillins, cephalosporins, and other, ⁇ -Lactam antibiotics, an agent comprising an aminoglycoside, protein synthesis inhibitors, drugs used in the chemotherapy of tuberculosis, mycobacterium avium complex disease, and leprosy, antifungal agents, antiviral agents including nonretro viral agents and antiretro viral agents.
  • therapeutic antibodies that can be combined with a subject compound include but are not limited to anti-receptor tyrosine kinase antibodies (cetuximab, panitumumab, trastuzumab), anti CD20 antibodies (rituximab, tositumomab), and other antibodies such as alemtuzumab, bevacizumab, and gemtuzumab.
  • anti-receptor tyrosine kinase antibodies cetuximab, panitumumab, trastuzumab
  • anti CD20 antibodies rituximab, tositumomab
  • other antibodies such as alemtuzumab, bevacizumab, and gemtuzumab.
  • therapeutic agents used for immunomodulation such as immunomodulators, immunosuppressive agents, tolerogens, and immunostimulants are contemplated by the methods herein.
  • therapeutic agents acting on the blood and the blood-forming organs such as hematopoietic agents, growth factors, minerals, and vitamins, anticoagulant, thrombolytic, and antiplatelet drugs.
  • the compounds described herein can be used in combination with the agents disclosed herein or other suitable agents, depending on the condition being treated. Hence, in some embodiments the compounds of the invention will be co-administered with other agents as described above.
  • the compounds described herein may be administered with the second agent simultaneously or separately.
  • This administration in combination can include simultaneous administration of the two agents in the same dosage form, simultaneous administration in separate dosage forms, and separate administration. That is, a compound described herein and any of the agents described above can be formulated together in the same dosage form and administered simultaneously. Alternatively, a compound of the present invention and any of the agents described above can be simultaneously administered, wherein both the agents are present in separate formulations.
  • a compound of the present invention can be administered just followed by and any of the agents described above, or vice versa.
  • a compound of the present invention and any of the agents described above may be administered a few minutes apart, or a few hours apart, or a few days apart.
  • the methods in accordance with the invention may include administering a c- met kinase selective inhibitor with one or more other agents that either enhance the activity of the inhibitor or compliment its activity or use in treatment. Such additional factors and/or agents may produce an augmented or even synergistic effect when administered with a c-met kinase selective inhibitor, or minimize side effects.
  • the methods of the invention may include administering formulations comprising a c-met kinase selective inhibitor of the invention with a particular cytokine, lymphokine, other hematopoietic factor, thrombolytic or anti-thrombotic factor, or anti-inflammatory agent before, during, or after administration of the c-met kinase inhibitor.
  • One of ordinary skill can easily determine if a particular cytokine, lymphokine, hematopoietic factor, thrombolytic of anti-thrombotic factor, and/or anti-inflammatory agent enhances or compliments the activity or use of the c-met kinase inhibitors in treatment.
  • the methods of the invention may comprise administering a c-met kinase selective inhibitor with one or more of TNF, IL-1, IL- 2, IL-3, IL4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, IL-14, IL-15, IL-16, IL- 17, IL-18, IFN, G-CSF, Meg-CSF, GM-CSF, thrombopoietin, stem cell factor, and erythropoietin.
  • Compositions in accordance with the invention may also include other known angiopoietins such as Ang-2, Ang4, and Ang-Y, growth factors such as bone morphogenic protein- 1, bone morphogenic protein-2, bone morphogenic protein-3, bone morphogenic protein-4, bone morphogenic protein-5, bone morphogenic protein-6, bone morphogenic protein-7, bone morphogenic protein- 8, bone morphogenic protein-9, bone morphogenic protein- 10, bone morphogenic protein-11, bone morphogenic protein- 12, bone morphogenic protein-13, bone morphogenic protein-14, bone morphogenic protein-15, bone morphogenic protein receptor I A, bone morphogenic protein receptor IB, brain derived neurotrophic factor, ciliary neutrophic factor, ciliary neutrophic factor receptor a, cytokine-induced neutrophil chemotactic factor 1, cytokine-induced neutrophil chemotactic factor 2 alpha, cytokine- induced neutrophil chemotactic factor 2 beta, beta endothelial cell growth factor, end
  • Representative compounds of the present invention include those specified above in Table 1 and pharmaceutically acceptable salts thereof.
  • the present invention also includes the intermediate compounds discussed in the examples and elsewhere in the specification as well as their salts. The present invention should not be construed to be limited to them.
  • the compounds of the present invention may be prepared by the following processes. Unless otherwise indicated, the variables (e.g. Cy 1 , R 2 , Li, L 2 , X, and Cy 2 ) when used in the below formulae are to be understood to present those groups described above in relation to formula (I).
  • Scheme 1 This scheme provides a method for the preparation of the compound of formula (IA) wherein L 2 is -CR a R b -, X is CR 1 or N and the other variables such as Cy 1 , R 2 , and Cy 2 are the same as described above in relation to formula (I).
  • the compound of formula (1) wherein Hal represents a halogen and R 2 is the same as described above in relation to formula (I) can be coupled with a compound of formula Cy 2 - L 2 -NH 2 in the presence of a suitable base, such as sodium or potassium carbonate, to give a compound of formula (2) wherein L 2 is -CR a R b -.
  • the compound of formula (2) can then be converted to a compound of formula (3) by reducing with a metal such as iron, or a metal halide such as stannous chloride and an acid (such as acetic acid, hydrochloric acid or ammonium chloride).
  • the compound of formula (5) can then be converted to a compound of formula (6) by reducing with a metal such as iron, or a metal halide such as stannous chloride and an acid such as acetic acid, hydrochloric acid or ammonium chloride.
  • Scheme IA This scheme provides a method for the preparation of the compound of formula (IA) wherein L 2 is -CR a R b -, X is CR 1 or N and the other variables such as Cy 1 , R 2 , and Cy 2 are the same as described above in relation to formula (I).
  • Compound of formula (la) can be converted to compound of formula (lb) using Ammonia or rectinf compound of formula (la) with a compound of formula -NHPg (wherein Pg is protecting group) under suitable conditions.
  • Compound of formula (la) can then be coupled with a compound of formula Cy 2 - L 2 -NH 2 or orcompound of formula (lb) can be coupled L 2 -NH 2 in the presence of a suitable base, such as sodium or potassium carbonate, to give a compound of formula (5) wherein L 2 is -CR a R b -.
  • the compound of formula (5) can then be converted to a compound of formula (6) by reducing with a metal such as iron, or a metal halide such as stannous chloride and an acid such as acetic acid, hydrochloric acid or ammonium chloride.
  • Scheme 2 This scheme provides a method for the preparation of a compoundormula (IA-I) wherein D is substituted or unsubstituted monocyclic aryl or substituted or unsubstituted monocyclic heteroaryl and the other variables such as L 2 , R 2 , X, and Cy 2 are the same as described above in relation to formula (IA-I):
  • a transition metal catalyst such as tetrakis(triphenylphosphine)palladium(0) and a suitable base such as potassium carbonate
  • Scheme 2 A This scheme provides an alternative method for the preparation of a compound of formula (IA-I) wherein D is substituted or unsubstituted monocyclic aryl or substituted or unsubstituted monocyclic heteroaryl and the other variables such as L 2 , R , X, and Cy 2 are the same as described above in relation to formula (IA-I):
  • a transition metal catalyst such as tetrakis(triphenylphosphine)palladium(0)
  • a suitable base such as potassium carbonate
  • Scheme 3 This scheme provides a method for the preparation of a compound of formula (IA-I) wherein D is phenyl substituted with -CONH-0-(CR x R y ) p -OR x , -CONH- (CR x R y ) p -OR x , -CONH-(CR x R y ) p -NHR y .
  • the phenyl ring is further substituted with one or more R' wherein each R is independently hydrogen, halogen or substituted or unsubstituted alkyl.
  • a transition metal catalyst such as tetrakis(triphenylphosphine)palladium(0) and a suitable base such as potassium carbonate
  • a suitable base such as potassium carbonate
  • the compound of formula (9) can be hydrolysed in the presence of an alkali metal hydroxide such as lithium hydroxide to give the compound of formula (10).
  • the compound of formula (10) can be converted into a compound of formula (IA-I) by reacting it with an amine of the formula R x R y NH in the presence of an amide coupling reagent such as N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC.HC1), (benzotriazol-lyl)oxytris(dimethylamino)phosphonium hexafluorophosphate (BOP) or any other amide coupling reagent known in the art.
  • an amide coupling reagent such as N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC.HC1), (benzotriazol-lyl)oxytris(dimethylamino)phosphonium hexafluorophosphate (BOP) or any other amide coupling reagent known in the art.
  • the conversion can be effected by reacting the compound of formula (10) with with a halogenating agent such as thionyl chloride and subsequently reacting the resultant acid halide with an amine of the formula NH 2 -0-(CR x R y ) p -OR x , NH 2 -(CR x R y ) p -OR x or NH 2 -(CR x R y ) p -NHR y in the presence of a suitable base such as a trialkylamine.
  • a halogenating agent such as thionyl chloride
  • the compounds of the present invention may be prepared by the following processes as disclosed in International Patent Application No. PCT/IB2011/052120, filed 13 th May 2011, and U.S. Patent Application No. 13/108,642 filed 16 th May 2011. These methods can similarly be applied to other compounds of formula as provided herein above with or without modification.
  • Stepl Quinoline-6-carboxylic acid: To a mixture of 4-aminobenzoic acid: (175 g, 1.28 mol), 4-nitrophenol (88.75 g, 0.64 mol) and sulphuric acid (1.2 lit.), glycerol (234.8 g, 2.55 mol) was added drop wise at 135°C. After 48h, the reaction mixture was cooled to 0°C and the pH adjusted to 3-5 with 10% sodium hydroxide solution. The resulting precipitate was collected by filtration and washed with water and dried under vacuum to afford the title compound as a black solid (125 g, 56%).
  • Step 2 Methyl quinoline-6-carboxylate: To a solution of quinoline-6-carboxylic acid (183 g, 1.06 mol) in methanol (1 lit.), thionyl chloride (150.7 g, 1.2 mol) was added drop wise at 0°C and then stirred at 65°C for 12h. The reaction mixture was concentrated and to the residue dichloromethane and aqueous sodium carbonate solutions were added. The organic layer was dried with sodium sulphate and concentrated to afford the title compound as a brown solid (150 g, 75%).
  • Step 3 Quinoline-6-carboxamide: To a solution of methyl quinoline-6-carboxylate (148 g, 0.79 mol) in methanol (600 ml), aqueous ammonia (800 ml) was added and then stirred at 45°C for 12h. The reaction mixture was concentrated to afford the title compound as a dark red solid (120 g, 88%).
  • Step 4 Quinoline-6-carbonitrile: To a solution of quinoline-6-carboxamide (177 g, 1.03 mol) in chloroform (1.5 lit.) triethylamine (520.15 g, 5.15 mol)and trifluoroacetic anhydride (540.34 g, 2.57 mol) was added drop wise below 10°C. After 1.5h, the pH was adjusted to 7 with sodium bicarbonate solution and extracted with dichloromethane. The organic layer was dried with sodium sulphate and concentrated to afford the title compound as a brown solid (96 g, 59%).
  • Step 5 Quinolin-6-ylmefhanamine: To a solution of quinoline-6-carbonitrile (96 g, 0.62 mol) in saturated ammonia in methanol (1 lit.), Raney-Ni (lOg) was added and the mixture was stirred at 1 atm of H 2 at RT for 16h. The reaction mixture was filtered and the filtrate was concentrated under vacuum to afford the title compound as a brown oil (80 g, 82%).
  • Step 1 6-Bromo-7-fluoroquinoline: To a mixture of 4-bromo-2-fluoroaniline (10 g, 52.62 mmol), ferrous sulphate (3.33 g, 11.97 mmol) and glycerol (15.78 ml) con. sulphuric acid (9.15 ml) was added slowly and the reaction mixture was heated to 140°C. After 12h, the reaction mixture was cooled to 0°C and the pH adjusted to 10-12 with 10% sodium hydroxide solution. The reaction mixture was filtered through celite, washed with ethyl acetate and layers were separated. The organic layer was washed with brine solution, dried over sodium sulphate and concentrated.
  • Step 2 7-Fluoroquinoline-6-carbonitrile: To a solution of 6-bromo-7-fluoroquinoline (4.90 g, 22.12 mmol) in dimethylacetamide (38 ml), potassium ferrocyanide (2.65 g, 4.86 mmol) and sodium carbonate (2.34 g, 22.12 mmol). The system was purged with nitrogen for 15 min. Palladium acetate (0.248 g, 1.10 mmol) was added under nitrogen and heated to 120°C. After 3h, the reaction mixture was filtered through celite, washed with ethyl acetate. The organic layer was washed with brine solution, dried over sodium sulphate and concentrated.
  • Step 3 (7-Fluoroquinolin-6-yl)methanamine: To 7-fluoroquinoline-6-carbonitrile (1.00 g, 5.813 mmol), methanol saturated with ammonia (13.5 ml) and Raney-Ni (1.27 g) were added and hydrogenated at 50-60 psi for 4h. The reaction mixture was filtered and concentrated to afford the title compound as a brown oil (0.80 g, 78%).
  • the title compound was obtained as a yellow solid (0.750 g, 50%) by using a procedure that is similar to the one described for intermediate 3 from 2,6-dichloro-3-nitropyridine (1.31 g, 6.81 mmol), Intermediate 2 (0.80 g, 4.54 mmol), ethanol (15 ml) and sodium carbonate (0.838 g, 7.90 mmol).
  • Tetrakis(triphenylphosphine)palladium(0) (0.040 g, 0.035 mmol) was added under nitrogen at RT and the reaction mixture was refluxed for 12h. The solvent was evaporated completely and water was added to the residue and extracted with ethyl acetate, dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by column chromatography with methanol: dichloromethane to afford the title compound as an off-white solid (0.100 g, 57%).
  • Step:2 4-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)benzoic acid: To a solution of intermediate 11 (0.095 g, 0.240 mmol) in methanol (1.4 ml), lithium hydroxide (0.028 g, 1.20 mmol) in water (0.36 ml) was added and stirred at RT. After 12h, the pH was adjusted to ca. 7.5 using 0.5N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as an off- white solid (0.070 g, 76%). M.P.: 245-247°C.
  • the title compound was prepared by following the procedure described for step 1 of Intermediate 11 using intermediate 7 (1.00 g, 3.07 mmol), 3-chloro-4- methoxycarbonylphenylboronic acid (0.825 g, 3.84 mmol), potassium acetate (0.976 g, 9.945 mmol), dioxan (20 ml) and tetrakis (triphenylphosphine)palladium(O) (0.284 g, 0.246 mmol). Reddish brown solid (1.00 g, 71%).
  • Step:2 2-Chloro-4-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)benzoic acid:
  • the title compound was prepared by following the procedure described for step 2 of Intermediate 11 using step 1 of Intermediate 12 (1.00 g, 2.18 mmol) in methanol (5 ml), lithium hydroxide (0.856 g, 20.40 mmol), water(5 ml), THF(19 ml). Off-white solid (0.900 g, 93%).
  • the acid was used without further purification in the next step.
  • Stepl 2-methylquinoline-6-carboxylic acid: To 4-aminobenzoic acid (5 g, 36.45 mmol) , 6N HCl (73 ml) was added and refluxed for 2h. Crotonaldehyde (3.06 g, 43.75 mmol) was added dropwise over 45 min.. After 12h, the reaction mixture was cooled to 0°C and the pH adjusted to 3-5 with aqueous ammonia solution. The aqueous layer containing solid was washed with dichloromethane and acidified with 2N HCl, filtered and dried under vacuum to afford the title compound as brown solid (3.0 g, 44%).
  • Step 2 methyl 2-methylquinoline-6-carboxylate: To a solution of 2-methylquinoline-6- carboxylic acid (3.0 g, 16.20 mmol) in methanol (30 ml.), sulphuric acid ( 3ml) was added dropwise at 0°C and then stirred at 65°C for 12h. The reaction mixture was concentrated and to the residue dichloromethane and aqueous sodium carbonate solutions were added. The organic layer was dried with sodium sulphate and concentrated to afford the title compound as a brown solid (1.9 g, 59%).
  • Step 3 2-methylquinoline-6-carboxamide: To a solution of methyl 2-methylquinoline-6- carboxylate (1.9 g, 9.44 mmol) in methanol (7.6 ml.), aqueous ammonia (10 ml) was added and then stirred at 45°C for 12h. The reaction mixture was concentrated to afford the title compound as a off-white red solid (1.0 g, 56%).
  • Step 4 2-methylquinoline-6-carbonitrile: To a solution of 2-methylquinoline-6-carboxamide (1.0 g, 5.36 mmol) in chloroform (5 ml.) and triethylamine (2.71 g, 26.84 mmol), trifluoroacetic anhydride (2.81 g, 13.42 mmol) was added dropwise below 10°C. After 1.5h, the pH was adjusted to 7 with sodium bicarbonate solution and extracted with dichloromethane. The organic layer was dried with sodium sulphate and concentrated to afford the title compound as a yellow solid (0.70 g, 77%).
  • Step 5 (2-methylquinolin-6-yl)methanamine: To a solution of 2-methylquinoline-6- carbonitrile (0.700 g, 4.16 mmol) in saturated ammonia in methanol (10 ml ), Raney-Ni (1.4g) was added and the mixture was stirred at 1 atm of 3 ⁇ 4 at RT for 16h. The reaction mixture was filtered and the filtrate was concentrated under vacuum to afford the title compound as a brown oil (0.700 g, 97%).
  • Step-1 6-chloro-N-((2-methylquinolin-6-yl)methyl)-3-nitropyridin-2-amine:
  • the title compound was obtained as a yellow solid (0.500 g, 38%) by using a procedure that is similar to the one described for intermediate 3 from 2,6-dichloro-3-nitropyridine (1.17 g, 6.09 mmol), Intermediate 13 (0.700 g, 4.06 mmol), ethanol (10 ml) and sodium carbonate (0.749 g, 7.07 mmol).
  • Step-2 6-chloro-N2-((2-methylquinolin-6-yl)methyl)pyridine-2,3-diamine:
  • the title compound was obtained as a off-white solid (0.500 g, 95%) by using a procedure that is similar to the one described for intermediate 5 from Step-1 (0.500 g, 1.52 mmol), stannous chloride (1.54 g, 6.85 mmol) and cone. HC1 (5.2 ml) which is used as such in next step.
  • Step-3 The title compound was obtained as a brown solid (0.400 g, 77%) by using a procedure that is similar to the one described for intermediate 7 from Step-2 (0.500 g, 1.67 mmol), acetic acid (2.94 ml), sodium nitrite (0.138 g, 2.03 mmol), water (0.8 ml) and sulphuric acid (0.2 ml) which is used as such in next step.
  • Stepl tert-butyl benzordlthiazol-6-ylmethylcarbamate: Triethylamine (2.92 ml, 20.82 mmol) and diphenylphosphoryl azide (5.72 g, 20.82 mmol) were added to a solution of benzothiazole-6-acetic acid (4.0 g, 20.82 mmol) in teri-butanol (80 ml) and refluxed for 18h. The excess tert-butanol was distilled out. Aq.
  • Step 2 benzordlthiazol-6-ylmethanamine: To a solution of tert-b tyl benzo[d]thiazol-6- ylmethylcarbamate (3.3 g, 12.48 mmol) in dioxane (33 ml), trifluoroacetic acid (8.25 ml) was added and stirred at RT for 3h. The reaction mixture was concentrated, basified with sodium hydroxide solution, extracted with ethyl acetate, the organic layers dried over sodium sulphate and concentrated under reduced pressure to afford the title compound as yellow solid (2.7 g) which was used as such for next step.
  • Step 3 N-(benzordlthiazol-6-ylmethyl)-6-chloro-3-nitropyridin-2-amine:
  • the title compound was obtained as a yellow solid (0.460 g, 9%) by using a procedure that is similar to the one described for intermediate 3 from 2,6-Dichloro-3-nitropyridine (4.75 g, 24.66 mmol), benzo[d]thiazol-6-ylmethanamine (2.70 g, 16.44 mmol), ethanol (50 ml) and sodium carbonate (3.03 g, 28.60 mmol) which was used as such for next step.
  • Step:4 N2-(benzordlthiazol-6-ylmethyl)-6-chloropyridine-2,3-diamine: The title compound was obtained as a yellow solid (0.360 g, 88%) by using a procedure that is similar to the one described for intermediate 5 from N-(benzo[d]thiazol-6-ylmethyl)-6-chloro-3-nitropyridin-2- amine (0.450 g, 1.40 mmol), stannous chloride (1.42 g, 6.31 mmol) and conc.HCl (7.5 ml) which is used as such for next step.
  • the title compound was obtained as a brown solid (0.068 g, 83%) by using a procedure that is similar to the one described for intermediate 7 from N2-(benzo[d]thiazol-6-ylmethyl)-6- chloropyridine-2,3-diamine (0.350 g, 0.249 mmol), acetic acid (1.75 ml), sodium nitrite (0.099 g, 1.44 mmol), water (0.8 ml) and sulphuric acid (0.4 ml).
  • Step-1 Methyl 2-chloro-4-(3-((7-fluoroquinolin-6-yl)methyl)-3H-ri,2,31triazolor4,5- blpyridin-5-yl)benzoate:
  • the title compound was prepared by following the procedure described for example 1 using intermediate 8 (0.345 g, 1.091 mmol), 3-chloro-4- methoxycarbonylphenylboronic acid (0.295 g, 1.37 mmol), potassium acetate (0.359 g, 3.65 mmol), dioxane (8 ml) and tetrakis(triphenylphosphine)palladium(0) (0.101 g, 0.087 mmol).
  • Step-2 2-Chloro-4-(3-((7-fluoroquinolin-6-yl)methyl)-3H-ri,2,31triazolor4,5-blpyridin-5- vDbenzoic acid: To a solution of Step-1 (0.185 g, 0.412 mmol) in methanol (2 ml), lithium hydroxide (0.161 g, 3.84 mmol) in water (2 ml) and THF (4 ml) were added and stirred at RT. After 12h, pH was adjusted to ca.
  • Step-1 Methyl 2,6-difluoro-4-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5- vDbenzoate: To a solution of Intermediate 7 (1.15 g, 3.91 mmol) and 3,5-difluoro-4- methoxycarbonylphenylboronic acid (prepared according to et. al in Eur. J. Org. Chem. 2009, 4325-4332, 1.10 g, 5.09 mmol) in dioxan (20 ml), potassium acetate (1.276 g, 13.03 mmol) was added and degassed for 30 min.
  • Tetrakis (triphenylphosphine)palladium(O) (0.361 g, 0.31346 mmol) was added under nitrogen at RT and the reaction mixture was refluxed for 12h. The solvent was evaporated completely and water was added to the residue and extracted with ethyl acetate, dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by column chromatography with methanol: dichloromethane to afford the title compound as a brown solid (0.620 g, 37%).
  • Step-2 2,6-Difluoro-4-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl) benzoic acid: To a solution of Step-1 (0.70 g, 1.62 mmol) in methanol (3.8 ml), lithium hydroxide (0.635 g, 15.13 mmol) in water (3.8 ml) and THF (14.3 ml) were added and stirred at RT. After 12h, pH was adjusted to ca. 7 using 0.5N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as pale brown solid (0.500 g, 74%). The acid was used as such for further steps.
  • Step-1 methyl 2,6-difluoro-4-(3-((7-fluoroquinolin-6-yl)methyl)-3H-ri,2,31triazolor4,5- blpyridin-5-yl)benzoate:
  • the title compound was prepared by following the procedure described for example 1 using intermediate 8 (0.750 g, 2.39 mmol), 3,5-difluoro-4- methoxycarbonylphenylboronic acid (0.569 g, 2.63 mmol), potassium acetate (0.783 g, 7.97 mmol), dioxane (17.2 ml) and tetrakis(triphenylphosphine)palladium(0) (0.221 g, 0.191 mmol). Brown solid (0.78 g, 76%) which is used as such in next step.
  • Step-2 To a solution of Step 2 (0.780 g, 1.73 mmol) in methanol (8.4 ml), lithium hydroxide (0.678 g, 16.17 mmol) in water (8.4 ml) and THF (17 ml) were added and stirred at RT. After 12h, pH was adjusted to ca. 7 using 0.5N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as a pale brown solid (0.600 g, 80%). The acid was used as such for further steps.
  • Step-1 Methyl 2-fluoro-4-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5- vDbenzoate:
  • the title compound was prepared by following the procedure described for example 1 using intermediate 7 (0.300 g, 1.01 mmol), 3-fluoro-4- methoxycarbonylphenylboronic acid (0.257 g, 1.29 mmol), potassium carbonate (0.466 g, 13.37 mmol), dioxan (6 ml), water (1.2 ml) and tetrakis (triphenylphosphine)palladium(O) (0.093 g, 0.081 mmol). Brown colour solid (0.300 g, 71%).
  • Step-2 To a solution of Step-1 (0.230 g, 0.556 mmol) in methanol (3.5 ml), lithium hydroxide (0.132 g, 5.56 mmol) in water(0.9 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 0.5N HCl and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as pale brown solid (0.130 g, 61%).M. : 254-257°C 'H-NMR ( ⁇ ppm, DMSO-d 6 , 400 MHz ):
  • Step-1 methyl 2-chloro-4-(3-((2-methylquinolin-6-yl)methyl)-3H-ri,2,31triazolor4,5- blpyridin-5-yl)benzoate:
  • the title compound was prepared by following the procedure described for Step-1 of Intermediate 17 using intermediate 14 (0.400 g, 1.29 mmol), 3- chloro-4-methoxycarbonylphenylboronic acid (0.304 g, 1.42 mmol), potassium acetate (0.422 g, 4.30 mmol), dioxan (8 ml) and tetrakis (triphenylphosphine)palladium(O) (0.119 g, 0.103 mmol). Brown colour solid (0.237 g, 41%) which is used as such in next step.
  • Step-2 2-chloro-4-(3-((2-methylquinolin-6-yl)methyl)-3H-ri,2,31triazolor4,5-blpyridin-5- vDbenzoic acid: To a solution of Step-1 (0.237 g, 0.556 mmol) in methanol (0.5 ml), THF (2.7 ml), lithium hydroxide (0.209 g, 4.98 mmol) in water(0.5 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 0.5N HCl and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as black solid (0.200 g, 87%). which is used as such in next step.
  • Step-1 methyl 4-(3-(benzordlthiazol-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)-2- chlorobenzoate:
  • the title compound was prepared by following the procedure described for Step-1 of intermediate 17 using intermediate 15 (0.400 g, 1.32 mmol), 3-chloro-4- methoxycarbonylphenylboronic acid (0.312 g, 1.45 mmol), potassium acetate (0.433 g, 4.41 mmol), dioxan (9.5 ml) and tetrakis (triphenylphosphine)palladium(O) (0.122 g, 0.106 mmol).
  • Step-2 To a solution of Step-1 (0.400 g, 0.917 mmol) in methanol (2.1 ml), THF (8.1 ml), lithium hydroxide (0.359 g, 8.56 mmol) in water(2.1 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 2N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as brown solid (0.370 g, 95%). MS (m/z): 422.1 (m + ).
  • Step-1 methyl 4-(3-(benzordlthiazol-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)-2,6- difluorobenzoate :
  • the title compound was prepared by following the procedure described for Step-1 of intermediate 17 using intermediate 15 (0.400 g, 1.32 mmol), 3,5-difluoro-4- methoxycarbonylphenylboronic acid (0.314 g, 1.45 mmol), potassium acetate (0.433 g, 4.41 mmol), dioxan (9.5 ml) and tetrakis (triphenylphosphine)palladium(O) (0.122 g, 0.106 mmol). Brown colour solid (0.380 g, 65%) which is used as such in next step.
  • Step-2 To a solution of Step-1 (0.380 g, 0.868 mmol) in methanol (1.9 ml), THF (7.6 ml), lithium hydroxide (0.340 g, 8.10mmol) in water (1.9 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 2N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as brown solid (0.340 g, 92%). MS (m/z): 424.2 (m + +l).
  • Step-1 methyl 4-(3-(benzordlthiazol-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)-2- fluorobenzoate:
  • the title compound was prepared by following the procedure described for Step-1 of intermediate 17 using intermediate 15 (0.300 g, 0.994 mmol), 3-fluoro-4- methoxycarbonylphenylboronic acid (0.197 g, 1.09 mmol), potassium acetate (0.324 g, 3.31 mmol), dioxan (7.1 ml) and tetrakis (triphenylphosphine)palladium(O) (0.091 g, 0.079 mmol). Brown colour solid (0.400 g, 95%) which is used as such in next step.
  • Step-2 To a solution of Step-1 (0.400 g, 0.952 mmol) in methanol (2.0 ml), THF (8.3 ml), lithium hydroxide (0.372 g, 8.88 mmol) in water (2.0 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 2N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as oof-white solid (0.300 g, 77%) which is used as such in next step.
  • Step-1 methyl 2,6-difluoro-4-(3-((2-methylquinolin-6-yl)methyl)-3H-ri,2,31triazolor4,5- blpyridin-5-yl)benzoate:
  • the title compound was prepared by following the procedure described for step-1 of intermediate 17 using intermediate 14 (0.500 g, 1.61 mmol), 3,5- difluoro-4-methoxycarbonylphenylboronic acid (0.383 g, 1.77 mmol), potassium acetate (0.527 g, 5.37 mmol), dioxan (11.5 ml) and tetrakis (triphenylphosphine)palladium(O) (0.149 g, 0.129 mmol). Brown colour solid (0.500 g, 69%) which is used as such in next step.
  • Step-2 To a solution of Step-1 (0.400 g, 0.898 mmol) in methanol (1.9 ml), THF (7.8 ml), lithium hydroxide (0.351 g, 8.37 mmol) in water (1.9 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 2N HCl and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as off-white solid (0.200 g, 51%) which is used as such in next step.
  • Step-1 Methyl 4-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-b1pyridin-5- yl)benzoate:The title compound was prepared by following the procedure described Step-1 for intermediate 17 using intermediate 7 (0.130 g, 0.439 mmol), 4- methoxycarbonylphenylboronic acid (0.100 g, 0.562 mmol), potassium carbonate (0.202 g, 1.46 mmol), dioxan (2.6 ml), water (0.5 ml) and tetrakis (triphenylphosphine)palladium(O) (0.040 g, 0.035 mmol). Off-white solid (0.100 g, 57%).
  • Step-2 To a solution of Step-1 (0.095 g, 0.240 mmol) in methanol (1.4 ml), lithium hydroxide (0.028 g, 1.20 mmol) in water (0.36 ml) was added and stirred at RT. After 12h, the pH was adjusted to ca. 7.5 using 0.5N HCl and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as an off-white solid (0.070 g, 76%).
  • Step-1 methyl 4-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)-2-
  • Step-2 To a solution of Step-1 (0.400 g, 0.863 mmol) in methanol (4 ml), THF (8.2 ml), lithium hydroxide (0.327 g, 8.05 mmol) in water (4 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 2N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as off-white solid (0.250 g, 64%) which is used as such in next step.
  • Step-1 methyl 4-(3-((7-fluoroquinolin-6-yl)methyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)-2- (trifluoromethyl)benzoate :
  • the title compound was prepared by following the procedure described for step-1 of intermediate 17 using intermediate 8 (0.400 g, 1.27 mmol), 3methyl 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)benzoate (0.464 g, 1.40 mmol), potassium acetate (0.417 g, 4.25 mmol), dioxan (9.6 ml) and tetrakis (triphenylphosphine)palladium(O) (0.118 g, 0.102 mmol). Brown colour solid (0.380 g, 62%) which is used as such in next step.
  • Step-2 To a solution of step-1 (0.400 g, 0.830 mmol) in methanol (1.8 ml), THF (7.2 ml), lithium hydroxide (0.325 g, 7.75 mmol) in water (1.8 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 2N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as off-white solid (0.300 g, 77%) which is used as such in next step.
  • Step-1 methyl 2-methyl-4-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5- yPbenzoate:
  • the title compound was prepared by following the procedure described for step-1 of intermediate 17 using intermediate 7 (0.290 g, 0.869 mmol), methyl 2-methyl-4- (4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benzoate (0.300 g, 1.08 mmol), potassium acetate (0.320 g, 3.26 mmol), dioxan (7.0 ml) and tetrakis (triphenylphosphine)palladium(O) (0.090 g, 0.078 mmol). Brown colour solid (0.250 g, 65%). which is used as such in next step.
  • Step-2 To a solution of Step-1 (0.250 g, 0.640 mmol) in methanol (5.5 ml), THF (2.5 ml), lithium hydroxide (0.250 g, 5.97 mmol) in water (2.5 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 2N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as off-white solid (0.120 g, 48%) which is used as such in next step.
  • Step-1 methyl 4-(3-((7-fluoroquinolin-6-yl)methyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)-2- methylbenzoate:
  • the title compound was prepared by following the procedure described for step-1 of intermediate 17 using intermediate 8 (0.303 g, 0.968 mmol), methyl 2-methyl-4- (4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benzoate (0.300 g, 1.08 mmol), potassium acetate (0.322 g, 3.28 mmol), dioxan (7.0 ml) and tetrakis (triphenylphosphine)palladium(O) (0.088 g, 0.077 mmol). Brown colour solid (0.250 g, 63%). which is used as such in next step.
  • Step-2 To a solution of step-1 (0.250 g, 0.610 mmol) in methanol (1.5 ml), THF (5.3 ml), lithium hydroxide (0.239 g, 5.69 mmol) in water (1.5 ml) was added and stirred at RT. After 12h, the pH was adjusted to 7-7.5 using 2N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as off-white solid (0.150 g, 59%) which is used as such in next step.
  • Step-l Methyl 2-fluoro-4-(3-((7-fluoroquinolin-6-yl)methyl)-3H-ri.2.31triazolor4.5- blpyridin-5-yl)benzoate:
  • the title compound was prepared by following the procedure described for step-1 of intermediate 17 using intermediate 8 (0.350 g, 1.15 mmol), 3-fluoro- 4-methoxycarbonylphenylboronic acid (0.276 g, 1.39 mmol), potassium acetate (0.365 g, 3.71 mmol), dioxane (8 ml) and tetrakis(triphenylphosphine)palladium(0) (0.103 g, 0.089 mmol). Pale brown solid (0.350 g, 70%).
  • Step-2 To a solution of step-1 (0.240 g, 0.605 mmol) in methanol (3 ml), lithium hydroxide (0.237 g, 5.64 mmol) in water (3 ml) and THF (6 ml) were added and stirred at RT. After 12h, pH was adjusted to ca. 7 using 0.5N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as pale brown solid (0.110 g, 44%). The acid was used as such for further steps.
  • Step:2 4-bromo-2,6-difluorobenzoic acid: To 4-bromo-2,6-difluorobenzaldehyde (4.0 g, 18.07 mmol) in DMF (80 ml), oxone (11.07 g, 18.07 mmol) was added and stirred at RT for 12h. The reaction mixture was quenched with 2N HC1 solution and extracted with ethyl acetate. The organic layer was dried over sodium sulphate and concentrated under vacuum to afford the title compound as an off-white solid (3.5 g , 83 %) which was used without characterisation in the next step.
  • Step:3 4-bromo-2,6-difluorobenzamide: To 4-bromo-2,6-difluorobenzoic acid (0.900 g, 3.81 mmol), thionyl chloride (9 ml) was added and refluxed for 3h. The excess thionyl chloride was removed under reduced pressure and the residue was cooled to 0°C. Aqueous 25% ammonia (7 ml) was added and stirred for 15 min. The precipitate formed was filtered and vacuum dried to afford title compound as an off-white solid (0.700 g, 78%) which was used without characterisation in the next step.
  • Step:4 2,6-difluoro-4-(4,4,5,5-tetramethyl-l ,3,2-dioxaborolan-2-yl)benzamide:
  • the title compound was obtained as a brown solid (0.500 g, 61 %) by using the procedure described for intermediate 9 from 4-bromo-2,6-difluorobenzamide (0.700 g, 2.92 mmol), bis(pinacolato)diboron (0.825 g, 3.22 mmol), potassium acetate (0.862 g, 8.75 mmol), dioxane (5 ml) and [l,l '-bis(diphenylphosphino)ferrocene]dichloro palladium(II).CH2Cl2 (0.071 g, 0.087 mmol).
  • Step: 1 4-bromo-2-chloro-N-methylbenzamide: To 4-bromo-2-chlorobenzoic acid (1.00 g, 4.24 mmol), thionyl chloride (10 ml) was added and refluxed for 3h. Excess thionyl chloride was removed under reduced pressure and the residue was cooled to 0°C. Methyl amine solution (25% in MeOH, 15 ml) was added and stirred for 15 min. The precipitate formed was filtered and vacuum dried to afford title compound as an off-white solid (0.900 g, 85%) which was used in the next step.
  • the title compound was obtained as a brown solid (0.600 g, 70%) by using the procedure described intermediate 9 from 4-bromo-2-methylbenzamide (0.700 g, 3.27 mmol), bis(pinacolato)diboron (0.913 g, 3.59 mmol), potassium acetate (0.96 g, 9.81 mmol), dioxane (12 ml) and [l, -bis(diphenylphosphino)ferrocene]dichloropalladium(II).CH 2 Cl2 (0.080 g, 0.098 mmol) which was used without characterisation in the next step.
  • Step:2 6-chloro-N2-(l-(quinolin-6-yl)ethyl)pyridine-2,3-diamine:
  • the title compound was obtained as a pale brown solid (0.600 g, 74%) by using a procedure that is similar to the one described for intermediate 5 from 6-Chloro-3-nitro-N-(l-(quinolin-6-yl)ethyl)pyridin-2- amine (0.900 g, 2.72 mmol), stannous chloride ( 2.77 g, 12.28 mmol) and conc.HCl (1.5 ml) which is used as such for next step.
  • the title compound was obtained as a yellow solid (0.050 g, 5%) by using a procedure that is similar to the one described for intermediate 3 from 2,6-Dichloro-3-nitropyridine (1.40 g, 7.73 mmol), (5,7-difluoroquinolin-6-yl)methanamine (1.00 g, 5.15 mmol), ethanol (10 ml) and sodium carbonate (0.97 g, 9.22 mmol).
  • Step: 2 6-chloro-N2-((5,7-difluoroquinolin-6-yl)methyl)pyridine-2,3-diamine:
  • the title compound was obtained as a brown solid (0.080 g, 73%) by using a procedure that is similar to the one described for intermediate 5 from 6-chloro-N-((5,7-difluoroquinolin-6-yl)methyl)- 3-nitropyridin-2-amine (0.12 g, 0.342 mmol), stannous chloride (0.347 g, 1.54 mmol) and conc.HCl (2 ml) which is used as such for next step.
  • Step 3 6-((5-chloro-3H-imidazo[4,5-b]pyridin-3-yl)methyl)-5,7-difluoroquinoline:
  • the title compound was obtained as a brown solid (0.150 g, 81%) by using a procedure that is similar to the one described for intermediate 34 from 6-chloro-N2- ((5,7-difluoroquinolin-6-yl) methyl) pyridine-2,3-diamine (0.180 g, 0.562 mmol), and formic acid (0.9 ml).
  • the title compound was obtained as a brown solid (0.800 g, 76%) by using a procedure that is similar to the one described for intermediate 31 from intermediate 8 (1.00 g, 3.18 mmol),dichloromethane (13 ml) and metachloroperbenzoic acid (1.10 g, 6.37 mmol) which was used as such in next step.
  • Step-1 methyl 2-fluoro-4-(3-(quinolin-6-ylmethyl)-3H-imidazor4,5-b1pyridin-5-yl)benzoate:
  • the title compound was prepared by following the procedure described for step-1 of intermediate 17 using intermediate 34 (1.00 g, 3.36 mmol), 3-fluoro-4- methoxycarbonylphenylboronic acid (0.734 g, 3.70 mmol), potassium acetate (1.11 g, 11.22 mmol), dioxane (24 ml) and tetrakis(triphenylphosphine)palladium(0) (0.311 g, 0.269 mmol). Pale brown solid (1.00 g, 76%).
  • Step-2 To a solution of step-1 (1.00 g, 2.42 mmol) in methanol (12 ml), lithium hydroxide (0.940 g, 22.62 mmol) in water (12 ml) and THF (24 ml) were added and stirred at RT. After 12h, pH was adjusted to ca. 7 using 0.5N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as off-white solid (0.600 g, 62%). The acid was used as such for further steps.
  • Step-1 methyl 2-methyl-4-(3-(quinolin-6-ylmethyl)-3H-imidazor4,5-blpyridin-5-yl)benzoate :
  • the title compound was prepared by following the procedure described for step-1 of intermediate 17 using intermediate 34 (1.00 g, 3.39 mmol), 3-methyl-4- methoxycarbonylphenylboronic acid (0.716 g, 3.73 mmol), potassium acetate (1.11 g, 11.29 mmol), dioxane (24 ml) and tetrakis(triphenylphosphine)palladium(0) (0.313 g, 0.271 mmol). Pale brown solid (0.800 g, 61%).
  • Step-2 To a solution of step-1 (0.800 g, 1.95 mmol) in methanol (9 ml), lithium hydroxide (0.766 g, 18.27 mmol) in water (9 ml) and THF (18 ml) were added and stirred at RT. After 12h, pH was adjusted to ca. 7 using 0.5N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as pale brown solid (0.600 g, 83%). The acid was used as such for further steps.
  • Step-1 methyl 2-chloro-4-(3-(quinolin-6-ylmethyl)-3H-imidazor4,5-b1pyridin-5-yl)benzoate:
  • the title compound was prepared by following the procedure described for step-1 of intermediate 17 using intermediate 34 (1.00 g, 3.39 mmol), 3-chloro-4- methoxycarbonylphenylboronic acid (0.715 g, 3.37 mmol), potassium acetate (1.11 g, 11.29 mmol), dioxane (24 ml) and tetrakis(triphenylphosphine)palladium(0) (0.313 g, 0.271 mmol). Pale brown solid (0.500 g, 35%).
  • Step-2 To a solution of step-1 (0.500 g, 1.16 mmol) in methanol (5.3 ml), lithium hydroxide (0.456 g, 10.86 mmol) in water (5.3 ml) and THF (10.7 ml) were added and stirred at RT. After 12h, pH was adjusted to ca. 7 using 0.5N HC1 and the solid precipitated was filtered, washed with ethyl acetate and petroleum ether and dried under vacuum to afford the title compound as pale brown solid (0.400 g, 82%). The acid was used as such for further steps.
  • the title compound was obtained as a brown solid (0.30 g, 50%) by using the procedure described in step 4 for intermediate 19 from intermediate 41 (0.500 g, 1.86 mmol), bis(pinacolato)diboron (0.705 g, 2.77 mmol), potassium acetate (0.743 g, 7.57 mmol), dioxane (4.6 ml) and [l,l '-bis(diphenylphosphino)ferrocene]dichloro palladium(II).CH 2 Cl 2 (0.061 g, 0.067 mmol) which is used as such for next step.
  • the title compound was obtained as a black solid (0.500 g, 53%) by using the procedure described intermediate 9 from 5-bromo-N-methylpicolinamide (0.900 g, 4.47 mmol), bis(pinacolato)diboron (1.25 g, 4.92 mmol), potassium acetate (1.31 g, 13.43 mmol), dioxane (13 ml) and [l, -bis(diphenylphosphino)ferrocene]dichloropalladium(II).CH 2 Cl2 (0.109 g, 0.134 mmol) which was used without characterisation in the next step.
  • Example 6d sodium (2-chloro-4-(3-(quinolin-6-ylmethyl)-3H-[l,2,3]triazolo[4,5-b]pyridin-5- yl)benzoyl)(2-hydroxyethoxy)amide: [273] To example 6 (0.100 g, 0.210 mmol) in isopropanol (2 ml) , 3N sodium hydroxide solution (0.076 ml) was added and stirred for 30 min. The reaction mixture was concentrated under reduced pressure. To the residue 1 ml isopropanol was added, filtered, washed with isopropanol, diethyl ether and dried under vacuum to afford the title compound as a yellow solid (0.080 g, 79 %).
  • the title compound was obtained as a pale green solid (0.020 g, 19%) by using a procedure that is similar to the one described for intermediate 31 from example 25 (0.100 g, 0.220 mmol),DMF (2.0 ml) and metachloroperbenzoic acid (0.189 g, 1.10 mmol). M.P.: 160-162°C.
  • Step-1 2-(l-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)ethylidene) hvdrazinecarboxamide : to a solution of intermediate 41 (0.070 g, 0.230 mmol) in ethnol (2 ml), sodium acetate (0.018 g, 0.230 mmol) and semicarbazide hydrochloride (0.026 g, 0.230 mmol) were added and stirred at RT for 12h. The reaction mixture was
  • Step-2 2-(l-(3-(quinolin-6-ylmethyl)-3H-ri,2,31triazolor4,5-blpyridin-5-yl)ethylidene) hvdrazinecarboxamide hydrochloride : the product of step-1 (0.050g, 0.138 mmol) was dissolved in THF (1 ml), eather saturated with HCl (0.15ml) was added at 0°C and stirred for 15 min. The precipitate formed was washed with eather and dried under vacuum to afford the title compound as an off-white solid (0.045 g, 82%).
  • Example 53 tert-butyl 2-(l-(3-(quinolin-6-ylmethyl)-3H-[l,2,3]triazolo[4,5-b]pyridin-5- yl)ethylidene) hydrazinecarboxylate : [336]
  • the title compound was prepared by following the procedure described for step-1 of Example 49 using intermediate 41 (0.200 g, 0.659 mmol), ethanol (5 ml) and tert-butyl carbazate (0.131 g, 0.989 mmol), heating at 60°C for 12h. Off-white solid (0.150g, 55 %).

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PCT/IB2013/051577 2012-03-30 2013-02-27 Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of c-met protein kinases WO2013144737A2 (en)

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CN201380022471.6A CN104321322A (zh) 2012-03-30 2013-02-27 作为c-met蛋白激酶调节剂的新型3,5-二取代-3h-咪唑并[4,5-b]吡啶和3,5-二取代-3h-[1,2,3]三唑并[4,5-b]吡啶化合物
KR1020147030532A KR20140144726A (ko) 2012-03-30 2013-02-27 C-met 단백질 키나제의 조절제로서의 신규한 3,5-디치환-3h-이미다조[4,5-b]피리딘 및 3,5- 디치환 -3h-[1,2,3]트리아졸로[4,5-b] 피리딘 화합물
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US14/389,336 US9815831B2 (en) 2012-03-30 2013-02-27 3,5-disubstituted-3H-imidazo[4,5-B]pyridine and 3,5-disubstituted-3H-[1,2,3]triazolo[4,5-B] pyridine compounds as modulators of c-Met protein kinases
CA2865719A CA2865719C (en) 2012-03-30 2013-02-27 Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of c-met protein kinases
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AP2014007966A AP3908A (en) 2012-03-30 2013-02-27 Novel 3,5-disubstituted-3H-imidazo[4,5-B]pyridine and 3,5-disubstituted-3H-[1,2,3]triazolo [4,5-B] pyridine compounds as modulators of C-met protein kinases
BR112014024251A BR112014024251A8 (pt) 2012-03-30 2013-02-27 novos compostos piridina 3,5-dissubstituída-3h-imidazo [4,5-b] e piridina 3,5-dissubstituída -3h-[1,2,3]triazolo[4,5-b] como moduladores de quinases de proteína c-met
SG11201406185WA SG11201406185WA (en) 2012-03-30 2013-02-27 Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of c-met protein kinases
ES13716061T ES2856848T3 (es) 2012-03-30 2013-02-27 Nuevos compuestos de 3,5-disustituida-3H-imidazo[4,5-B] biridina y 3,5-disustituida-3H-[1,2,3] triazolo[4,5-B] piridina como moduladores de proteína cinasas C-MET
JP2015502481A JP6192708B2 (ja) 2012-03-30 2013-02-27 Ｃ−ｍｅｔプロテインキナーゼ調節物質としての新規３，５−二置換−３ｈ−イミダゾ［４，５−ｂ］ピリジン化合物および３，５−二置換−３ｈ−［１，２，３］トリアゾロ［４，５−ｂ］ピリジン化合物
KR1020207002779A KR102164317B1 (ko) 2012-03-30 2013-02-27 C-met 단백질 키나제의 조절제로서의 신규한 3,5-디치환-3h-이미다조[4,5-b]피리딘 및 3,5- 디치환 -3h-[1,2,3]트리아졸로[4,5-b] 피리딘 화합물
EP13716061.0A EP2831073B1 (en) 2012-03-30 2013-02-27 Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b]pyridine compounds as modulators of c-met protein kinases
IL234513A IL234513B (en) 2012-03-30 2014-09-07 Novel 3,5-disubstituted-3h-imidazo[4,5-b]pyridine and 3,5-disubstituted-3h-[1,2,3]triazolo[4,5-b]pyridine compounds as modulators of c-met protein kinases
PH12014502166A PH12014502166B1 (en) 2012-03-30 2014-09-26 Novel 3,5-disubstituted-3h-imidazo[4,5-b]pyridine and 3,5- disubstituted -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of c-met protein kinases
HK15105126.9A HK1204612A1 (en) 2012-03-30 2015-05-29 Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b]pyridine compounds as modulators of c-met protein kinases c-met 35--3h-[45-b] 3 5--3h-[123][45-b]
US15/705,005 US11066402B2 (en) 2012-03-30 2017-09-14 3,5-disubstituted-3H-imidazo[4,5-b]pyridine and 3,5-disubstituted-3H-[1,2,3]triazolo[4,5-B] pyridine compounds as modulators of c-Met protein kinases
US17/303,494 US20210371416A1 (en) 2012-03-30 2021-05-30 Novel 3,5-disubstituted-3h-imidazo[4,5-b]pyridine and 3,5- disubstituted -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of c-met protein kinases

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